FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL

K Number: K792016 · Decision Oct 26, 1979
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
112
Applicant Total
5
Review Days
21

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
DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL
K Number
K792016
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Arbrook Mfg. Corp.
Date Received
October 5, 1979
Decision Date
October 26, 1979
Product Code
MMK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
MMK Container, Sharps

Similar 510(k) Clearances

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

View all

Other Clearances by Arbrook Mfg. Corp.

K Number Device Name
K781847 LATEX, IN-HOUSE COMPOUNDED
K781278 GLOVES, PROCEDURE
K770056 GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE
K760421 THERMOMETER, SURVALENT-ELECTRONIC