Atlas FDA

WIPEABLE PILLOW

FDA 510(k) clearance K924477 · decided 1993-01-29

Clearance details

K-number
K924477
Device name
WIPEABLE PILLOW
Applicant
Perfect Fit Industries, Inc.
Decision
Substantially Equivalent
Date received
1992-09-03
Decision date
1993-01-29
Days to decision
148 days
Clearance type
Traditional
Product code
FMW
Device class
1
Regulation number
880.6190
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Charlotte, NC, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.