FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DEXIDE DISPOSABLE SURGICAL SCRUB BRUSH

K Number: K791952 · Decision Oct 17, 1979
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
36
Applicant Total
38
Review Days
16

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DEXIDE DISPOSABLE SURGICAL SCRUB BRUSH
K Number
K791952
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dexide, Inc.
Date Received
October 1, 1979
Decision Date
October 17, 1979
Product Code
GEC
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEC Brush, Scrub, Operating-Room

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEC), ordered by most recent decision date.

View all

Other Clearances by Dexide, Inc.

K Number Device Name
K991814 MULTACHOICE INSTRUMENTS
K990379 MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES
K981940 MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES
K981941 MULTAPORT CANNULA REDUCER AND ACCESSORIES
K953611 DEXIDE ENDO-LUBE KIT
K944509 DEXIDE INSUFFLATION TUBING WITH FILTER
K924117 DEXIDE LAPAROSCOPIC KITS
K923845 DEXIDE LAPAROSCOPIC ACCESSORIES
K921709 ENDOBAG, MODIFICATION
K913762 MONOSCOPY(TM) BRAND, ENDOBAG
Search all 38 clearances from Dexide, Inc. →