VIEWSCAN
FDA 510(k) clearance K863994 · decided 1986-10-31
Clearance details
- K-number
- K863994
- Device name
- VIEWSCAN
- Applicant
- Sensory Aids Corp.
- Decision
- Substantially Equivalent
- Date received
- 1986-10-14
- Decision date
- 1986-10-31
- Days to decision
- 17 days
- Clearance type
- Traditional
- Product code
- HOT
- Device class
- 1
- Regulation number
- 886.5910
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Bensenville, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Sensory Aids Corp.
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 |
|---|---|---|
| SPECTACLE, MAGNIFYING (K873967) | Swank Plus , Ltd. | 1988-02-26 |
Recalls involving this device
No recalls on record reference this clearance.