RULE, PUPILLARY
FDA 510(k) clearance K873440 · decided 1987-09-21
Clearance details
- K-number
- K873440
- Device name
- RULE, PUPILLARY
- Applicant
- Allegheny Plastics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-08-27
- Decision date
- 1987-09-21
- Days to decision
- 25 days
- Clearance type
- Traditional
- Product code
- HMM
- Device class
- 1
- Regulation number
- 886.1190
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Coraopolis, PA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Allegheny Plastics
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| DISTOMETER (K882575) | Hagg-Streit Service, Inc. | 1988-07-01 |
Recalls involving this device
No recalls on record reference this clearance.