VTS REPORTER OR VTS LINK
FDA 510(k) clearance K863993 · decided 1986-10-31
Clearance details
- K-number
- K863993
- Device name
- VTS REPORTER OR VTS LINK
- 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
- HPF
- Device class
- 1
- Regulation number
- 886.5900
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Bensenville, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.