510(k) K920271
- Device
- WEINSTEIN CORNEAL MIRCOAESTHESIOMETER
- Applicant
- CONNECTICUT BIOINSTRUMENTS, INC.
- 510(k) number
- K920271
- Product code
- HJC
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1992-04-21
- Date received
- 1992-01-22
- Regulation
- 886.1040
- Classification name
- Esthesiometer, Ocular
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- No
Applicant Contact#
- Contact
- CURT WEINSTEIN
- Address
- 5 B Oak Ln. Danbury CT US 06811 06811
FDA Registration Numbers#
- 3023271442
- 3009173773
- 3009420598
- 8040278
- 3042228518
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HJC #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K851557 | ANESTHESIOMETER | Luneau SA | 1985-05-30 |
Legacy Summary#
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FDA Review#
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