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FDA Product Code

FDA Product Code GDY — Clearance Directory

Device Class
Class I
21 CFR Citation
878.4450

510(k) Clearances — 111 records · page 2 of 2

K-Number Device Name Applicant Decision Date Clearance Type Summary
K800102 STANFORD STERILE LAP SPONGES Lukens Corp. 1980-01-28 Traditional PDF ↗
K792630 STERILIZATION PROCESS/X-RAY DETECT. SPG Procter & Gamble Mfg. Co. 1980-01-11 Traditional PDF ↗
K792471 STANFORD STERILE LAP SPONGES Lukens Corp. 1979-12-20 Traditional PDF ↗
K790389 GAUZE & COTTON SPONGES Medtech Intl., Inc. 1979-03-26 Traditional PDF ↗
K782107 LAP SPONGE Carapace, Inc. 1979-02-16 Traditional PDF ↗
K790050 SPONGES, STANFORD STERILE LAP Stanford Professional Products 1979-01-17 Traditional PDF ↗
K781818 LAPARATOMY SPONGE Meden Medical Sales Division 1978-11-15 Traditional PDF ↗
K780718 SOF-WICKLAP PAD Johnson & Johnson Professionals, Inc. 1978-06-28 Traditional PDF ↗
K780871 ARTERIAL LINE KIT Argon Medical Corp. 1978-06-14 Traditional PDF ↗
K771395 LAPAROTOMY SPONGES, STERILE Medline Industries, Inc. 1977-08-19 Traditional PDF ↗
K770924 GREEN RADIOPAQUE IN SURG. SPONGES Kendall Research Center 1977-08-10 Traditional PDF ↗

Product code GDY · Class I · General, Plastic Surgery. Data: openFDA.