PARAGON MICRO-LOOPS
FDA 510(k) clearance K860022 · decided 1986-03-24
Clearance details
- K-number
- K860022
- Device name
- PARAGON MICRO-LOOPS
- Applicant
- Paragon Medical and Scientific, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-01-03
- Decision date
- 1986-03-24
- Days to decision
- 80 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Saint Paul, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.