Atlas FDA

PROCEDURE & RECOVERY PATIENT SUIT

FDA 510(k) clearance K803171 · decided 1981-03-04

Clearance details

K-number
K803171
Device name
PROCEDURE & RECOVERY PATIENT SUIT
Applicant
Alba Health Care
Decision
Substantially Equivalent
Date received
1980-12-15
Decision date
1981-03-04
Days to decision
79 days
Clearance type
Traditional
Product code
FYB
Device class
2
Regulation number
878.4040
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
DISPOSABLE ISOLATION GOWN (K911921)Liaoning-Usa Corp.1991-05-13
DISPOSABLE MEDICAL GOWNS (K891820)Bioshield, Inc.1989-07-24
DENTAL BIB (K891053)Dispomed, Inc.1989-04-12
SHIELD DISP. PATIENTS PONCHO GOWNS (K801570)American Convertors Div., American Pharmaseal1980-07-28
PEDIATRICS GOWN (K771929)Convertors1977-11-16

Recalls involving this device

No recalls on record reference this clearance.