Atlas FDA

APRONS, SCRUBS SLACKS & TOPS, PATIENT DRAPE

FDA 510(k) clearance K891212 · decided 1989-04-14

Clearance details

K-number
K891212
Device name
APRONS, SCRUBS SLACKS & TOPS, PATIENT DRAPE
Applicant
Pro-Safe Professional Linens, Inc.
Decision
Substantially Equivalent
Date received
1989-03-07
Decision date
1989-04-14
Days to decision
38 days
Clearance type
Traditional
Product code
FXO
Device class
1
Regulation number
878.4040
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Grand Junction, CO, 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
BTP(TM) CENTRALINE(TM) SUIT (K914615)Btp Industries, Inc.1992-05-05
SUIT, SURGICAL (K882282)A Plus International, Inc.1988-06-23
SURGICAL GARMENTS (K865022)Ulti-Med Intl., Inc.1987-01-12
SPUNGUARD SCRUB SUIT (K831207)Kimberly-Clark Corp.1983-05-16
MULTIPLE SCRUB SUIT (K822483)Surgilite Intl., Inc.1982-09-17

Recalls involving this device

No recalls on record reference this clearance.