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 15, 2026, FDA's public records list Medical Technical Products with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 28, 1994: STANDARD PHACO TIP 15, 30, 45, 60.
| Sep 28, 1994 | STANDARD PHACO TIP 15, 30, 45, 60K940083 · HQC | 510(k) clearances |
| Aug 4, 1994 | MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECEK940088 · HQC | 510(k) clearances |
| Jun 17, 1994 | MODEL 2000 OPHTHALMIC SURGICAL SYSTEMK940084 · HQC | 510(k) clearances |
| Mar 13, 1991 | MTP TRANSPORT INFUSION PUMP, MODEL NO. MTPLEAK910335 · FRN | 510(k) clearances |
| Feb 7, 1991 | MTP TRANSPORT INFUSION PUMP MODEL NO. 1001AK905251 · FRN | 510(k) clearances |
| Dec 26, 1990 | I/A-PHACO SYSTEM (IRR./ASPIR./AND PHACO./SYSTEM)K904612 · HQC | 510(k) clearances |
| Aug 10, 1987 | PART #860070 ULTRAPAK & #860075 ULTRAPAKK871474 · HOC | 510(k) clearances |
| Aug 10, 1987 | PART #860065 IA PAK & PART #860060 IA PAKK871473 · HQC | 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
