SAFESHARPE (TM) DISPOSAL SYSTEM
FDA 510(k) clearance K925056 · decided 1995-04-21
Clearance details
- K-number
- K925056
- Device name
- SAFESHARPE (TM) DISPOSAL SYSTEM
- Applicant
- Life Medical Technologies, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1992-10-06
- Decision date
- 1995-04-21
- Days to decision
- 927 days
- Clearance type
- Traditional
- Product code
- FMI
- Device class
- 2
- Regulation number
- 880.5570
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- 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.