510(k) K873554
- Device
- Gorsk Instrument Rest
- Applicant
- GORSK, INC.
- 510(k) number
- K873554
- Product code
- HMG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1987-10-23
- Date received
- 1987-08-28
- Regulation
- 886.1860
- Classification name
- Stand, Instrument, Ophthalmic, Non-Powered
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- NANCY G GORSKI
- Address
- P.O. Box 398 Camarillo CA US 93011 93011
FDA Registration Numbers#
- 9612297
- 3005955744
- 9680168
- 8040381
- 3010675798
- 8040382
- 9680718
- 1528142
- 3010673832
- 3010755771
- 8040278
- 1418300
- 3003951061
- 9613083
- 3005440795
Source Documents#
510(k) summary PDF not indicated by FDA