SKIN SCRUB KIT
FDA 510(k) clearance K890570 · decided 1989-05-05
Clearance details
- K-number
- K890570
- Device name
- SKIN SCRUB KIT
- Applicant
- Kit Pak, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-02-06
- Decision date
- 1989-05-05
- Days to decision
- 88 days
- Clearance type
- Traditional
- Product code
- LRO
- Device class
- 2
- Regulation number
- 878.4370
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Elk Grove Village, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.