The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Insulated Forceps, Biopsy Forceps, Scissors.
Device ID | K935071 |
510k Number | K935071 |
Device Name: | INSULATED FORCEPS, BIOPSY FORCEPS, SCISSORS |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. 1201 ROBERTS BLVD. Kennesaw, GA 30144 |
Contact | Paul L Sumner |
Correspondent | Paul L Sumner KARL STORZ ENDOSCOPY-AMERICA, INC. 1201 ROBERTS BLVD. Kennesaw, GA 30144 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-10-25 |
Decision Date | 1994-04-25 |