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 13, 2026, FDA's public records list Pro-Tech, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 4, 1995: BODY POSITION INDICATOR, MODEL BPI1.
| Date | Record | Source |
|---|---|---|
| May 4, 1995 | BODY POSITION INDICATOR, MODEL BPI1K940013 · MNR | 510(k) clearances |
| Jan 11, 1995 | SNORING MICROPHONE, SM1K940015 · MNR | 510(k) clearances |
| Nov 10, 1994 | PLM SENSOR, MODEL PLM1K940014 · BZQ | 510(k) clearances |
| Sep 10, 1993 | FREEDOM OXIMETER/EEG DIGITAL INTERFACEK924752 · DQA | 510(k) clearances |
| Dec 30, 1992 | CRYSTAL TRACE PIEZO RESPIRATORY EFFORT SENSORK923402 · BZQ | 510(k) clearances |
| May 22, 1992 | CANNULA STYLE THERMOCOUPLESK913396 · BZG | 510(k) clearances |
| May 20, 1992 | EZ-1 SYSTEM RESPIRATORY EFFORT SENSORSK913395 · BZG | 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
