MARCO STANDARD RADIUSGAUGES
FDA 510(k) clearance K930437 · decided 1993-08-09
Clearance details
- K-number
- K930437
- Device name
- MARCO STANDARD RADIUSGAUGES
- Applicant
- Marco Ophthalmic, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1993-01-26
- Decision date
- 1993-08-09
- Days to decision
- 195 days
- Clearance type
- Traditional
- Product code
- HLF
- Device class
- 1
- Regulation number
- 886.1430
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Jacksonville, FL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| BAUSCH & LOMB CONTACT LENS VIEWER (K862517) | Bausch & Lomb, Inc. | 1986-08-11 |
| ERG-JET ELECTRODE (K823767) | Life-Tech Intl., Inc. | 1983-01-08 |
Recalls involving this device
No recalls on record reference this clearance.