HGM ENDOCOAGULATOR MODEL 8
FDA 510(k) clearance K851651 · decided 1985-07-23
Clearance details
- K-number
- K851651
- Device name
- HGM ENDOCOAGULATOR MODEL 8
- Applicant
- Hgm, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1985-04-22
- Decision date
- 1985-07-23
- Days to decision
- 92 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Salt Lake City, UT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.