INTERP-1000
FDA 510(k) clearance K921476 · decided 1992-10-21
Clearance details
- K-number
- K921476
- Device name
- INTERP-1000
- Applicant
- Qmed, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1992-03-30
- Decision date
- 1992-10-21
- Days to decision
- 205 days
- Clearance type
- Traditional
- Product code
- LOS
- Advisory committee
- Unknown
- Location
- Laurence Harbor, NJ, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.