GLOBE RES-Q-FLO
FDA 510(k) clearance K834128 · decided 1983-12-29
Clearance details
- K-number
- K834128
- Device name
- GLOBE RES-Q-FLO
- Applicant
- Globe Safety Equipment, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1983-11-29
- Decision date
- 1983-12-29
- Days to decision
- 30 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.