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 |