510(k) K924198
- Device
- MODIFIED SITE FIBER OPTIC MODULE
- Applicant
- CHIRON VISION CORP.
- 510(k) number
- K924198
- Product code
- FCT
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1992-11-23
- Date received
- 1992-08-20
- Regulation
- 886.4335
- Classification name
- Headlight, Fiberoptic Focusing
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- BRUNT MILLER
- Address
- 135 Gibraltar Rd. Horsham PA US 19044 19044
FDA Registration Numbers#
- 1000379039
- 3004001706
- 3031231776
- 1926681
- 2434839
- 3011137372
- 1222275
- 9611102
- 3021839632
- 3007532396
- 1054713
- 3005216736
- 3012185136
- 1037039
- 9680718
- 3010041511
- 1450019
- 1058726
Source Documents#
Other 510(k) Records For Product Code FCT #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K960767 | LIGHT COMMANDER | Scieran Technologies, Inc. | 1996-08-26 |
| K883480 | MODIFIED SITE FIBER OPTIC MODULE FOR OPHTHAL. USE | Site Microsurgical Systems, Inc. | 1988-08-24 |
| K802769 | FIBER OPTIC HEADLIGHT #60-0765 | Aspen Laboratories, Inc. | 1980-12-11 |
| K802770 | FIBER OPTIC HEADLIGHT #60-0766766 | Aspen Laboratories, Inc. | 1980-12-11 |
| K780433 | FIBER OPTIC ADJUSTABLE HEADLIGHT | Cameron-Miller, Inc. | 1978-06-13 |
Legacy Summary#
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FDA Review#
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