The following data is part of a premarket notification filed by Solos Endoscopy, Inc. with the FDA for Gs-1000 Grasping Forcep, 5mm, Insulated.
Device ID | K900947 |
510k Number | K900947 |
Device Name: | GS-1000 GRASPING FORCEP, 5MM, INSULATED |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | SOLOS ENDOSCOPY, INC. 6191 ATLANTIC BLVD. SUITE 4 Norcross, GA 30071 |
Contact | Leila H Holmes |
Correspondent | Leila H Holmes SOLOS ENDOSCOPY, INC. 6191 ATLANTIC BLVD. SUITE 4 Norcross, GA 30071 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-02-27 |
Decision Date | 1990-04-18 |