TRIANGULAR BANDAGE
FDA 510(k) clearance K870284 · decided 1987-02-24
Clearance details
- K-number
- K870284
- Device name
- TRIANGULAR BANDAGE
- Applicant
- The Medical Group, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-01-27
- Decision date
- 1987-02-24
- Days to decision
- 28 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Reno, NV, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.