Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Sun Biomedical Laboratories with 17 510(k) clearances. The most recent is a 510(k) clearance dated Aug 25, 2003: VISUALINE METHADONE DIPSTRIPTEST.
| Aug 25, 2003 | VISUALINE METHADONE DIPSTRIPTESTK023856 · DJR | 510(k) clearances |
| May 6, 2003 | VISUALINE CUP IV FOR DRUGS OF ABUSE TEST FOR QUALITATIVE DETERMINATION OF COCAINE, CANNABINOIDS, MORPHINE, METHAMPHETAMIK023648 · LDJ | 510(k) clearances |
| Apr 25, 2002 | VISUALINE II (ALSO KNOWN AS SUNLINE) BARITURATESK014089 · DIS | 510(k) clearances |
| Mar 20, 2002 | VISUALINE BARBITURATES DIPSTRIP TESTK020136 · DIS | 510(k) clearances |
| Jul 17, 2001 | VISUALINE AMPHETAMINE DIPSTRIP ASSAYK011499 · DKZ | 510(k) clearances |
| May 17, 2001 | VISUALINE II (ALSO KNOWN AS SUNLINE) AMPHETAMINE ASSAYK010177 · DKZ | 510(k) clearances |
| Dec 27, 1999 | VISUALINE V DRUGS OF ABUSE DIPSTRIP PANEL FOR QUALITATIVE DETERMINATION OF COCAINE, CANNABINOIDS, MORPHINE, METHAMPEK993485 · DIO | 510(k) clearances |
| Mar 1, 1999 | VISUALINE II (ALSO KNOWN AS SUNLINE) PHENCYCLIDINEK983790 · LCM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
