SURGICAL PLASTERS
FDA 510(k) clearance K861695 · decided 1986-08-01
Clearance details
- K-number
- K861695
- Device name
- SURGICAL PLASTERS
- Applicant
- Salvaplast Industries
- Decision
- Substantially Equivalent
- Date received
- 1986-05-02
- Decision date
- 1986-08-01
- Days to decision
- 91 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- 49 348, Israel, IL
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.