510(k) K772394
- Device
- KALRN FACE-LIFE SCISSORS
- Applicant
- EDWARD WECK, INC.
- 510(k) number
- K772394
- Product code
- FZI
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-03-09
- Date received
- 1977-12-27
- Regulation
- 878.5070
- Classification name
- Apparatus, Air Handling, Enclosure
- Medical specialty
- General & Plastic Surgery
- Review panel
- General & Plastic Surgery
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3016750643
- 3044563550
- 1526611
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FZI #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K911132 | MULTIPLE, SURGICAL DRAPE PACK | Central Georgia Ancillary Health Systems | 1991-05-06 |
| K910468 | STERILE DISPOSABLE DRAPE(S) | E.M. Adams | 1991-03-21 |
| K854159 | ELLIPTI-PUNCH | Alcon Laboratories | 1985-11-15 |
| K772395 | DAVIS RHYTIDECTOMY | Edward Weck, Inc. | 1978-03-09 |
Legacy Summary#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases
FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases