The following data is part of a premarket notification filed by Richards Medical Co., Inc. with the FDA for Endoscopes For Sinus Surgery.
| Device ID | K874215 |
| 510k Number | K874215 |
| Device Name: | ENDOSCOPES FOR SINUS SURGERY |
| Classification | Nasopharyngoscope (flexible Or Rigid) |
| Applicant | RICHARDS MEDICAL CO., INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Contact | Robert F Games |
| Correspondent | Robert F Games RICHARDS MEDICAL CO., INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Product Code | EOB |
| CFR Regulation Number | 874.4760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-16 |
| Decision Date | 1988-01-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00821925027169 | K874215 | 000 |
| 00821925026360 | K874215 | 000 |
| 00821925026377 | K874215 | 000 |
| 00821925026384 | K874215 | 000 |
| 00821925026391 | K874215 | 000 |
| 00821925026407 | K874215 | 000 |
| 00821925026414 | K874215 | 000 |
| 00821925027114 | K874215 | 000 |
| 00821925027121 | K874215 | 000 |
| 00821925027138 | K874215 | 000 |
| 00821925027145 | K874215 | 000 |
| 00821925027152 | K874215 | 000 |
| 00821925025325 | K874215 | 000 |