STERILITE STERILIZATION KIT
FDA 510(k) clearance K864596 · decided 1986-12-18
Clearance details
- K-number
- K864596
- Device name
- STERILITE STERILIZATION KIT
- Applicant
- Kimberly-Clark Corp.
- Decision
- Substantially Equivalent
- Date received
- 1986-11-21
- Decision date
- 1986-12-18
- Days to decision
- 27 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Roswell, GA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.