The following data is part of a premarket notification filed by R. A. Fischer Co. Corp. with the FDA for Cb-7 Electronic Epilator.
Device ID | K871372 |
510k Number | K871372 |
Device Name: | CB-7 ELECTRONIC EPILATOR |
Classification | Epilator, High Frequency, Needle-type |
Applicant | R. A. FISCHER CO. CORP. 517 COMMERCIAL ST. Glendale, CA 91203 |
Contact | Van Orden |
Correspondent | Van Orden R. A. FISCHER CO. CORP. 517 COMMERCIAL ST. Glendale, CA 91203 |
Product Code | KCW |
CFR Regulation Number | 878.5350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-04-07 |
Decision Date | 1987-04-28 |