The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Operating Laryngoscopes & Accessories Forceps, Protectors.
Device ID | K953771 |
510k Number | K953771 |
Device Name: | OPERATING LARYNGOSCOPES & ACCESSORIES FORCEPS, PROTECTORS |
Classification | Nasopharyngoscope (flexible Or Rigid) |
Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
Contact | Lydia N Telep |
Correspondent | Lydia N Telep KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
Product Code | EOB |
CFR Regulation Number | 874.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-08-14 |
Decision Date | 1995-11-22 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04048551169711 | K953771 | 000 |
04048551169704 | K953771 | 000 |