The following data is part of a premarket notification filed by Geiger Medical Technologies, Inc. with the FDA for Geiger Electrosurgical Handpiece Sheath, Model 405.
| Device ID | K992149 |
| 510k Number | K992149 |
| Device Name: | GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | GEIGER MEDICAL TECHNOLOGIES, INC. 24040 CAMINO DEL AVION, A-195 Monarch Beach, CA 92629 |
| Contact | John Bottjer |
| Correspondent | John Bottjer GEIGER MEDICAL TECHNOLOGIES, INC. 24040 CAMINO DEL AVION, A-195 Monarch Beach, CA 92629 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-06-24 |
| Decision Date | 1999-08-19 |
| Summary: | summary |