ARGON FIBER OPTIC CATHETER
FDA 510(k) clearance K827847 · decided 1983-01-03
Clearance details
- K-number
- K827847
- Device name
- ARGON FIBER OPTIC CATHETER
- Applicant
- Hgm, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-11-04
- Decision date
- 1983-01-03
- Days to decision
- 60 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.