The following data is part of a premarket notification filed by Frigitronics Of Connecticut, Inc. with the FDA for Cs-76 And/or Cryocare I.
| Device ID | K760742 |
| 510k Number | K760742 |
| Device Name: | CS-76 AND/OR CRYOCARE I |
| Classification | Unit, Cryosurgical, Accessories |
| Applicant | FRIGITRONICS OF CONNECTICUT, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | GEH |
| CFR Regulation Number | 878.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-09-30 |
| Decision Date | 1976-11-03 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00888937011111 | K760742 | 000 |
| 00888937010992 | K760742 | 000 |
| 00888937011005 | K760742 | 000 |
| 00888937011012 | K760742 | 000 |
| 00888937011029 | K760742 | 000 |
| 00888937011036 | K760742 | 000 |
| 00888937011067 | K760742 | 000 |
| 00888937011074 | K760742 | 000 |
| 00888937011081 | K760742 | 000 |
| 00888937011098 | K760742 | 000 |
| 00888937011104 | K760742 | 000 |
| 00888937010985 | K760742 | 000 |