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

SHARPS DISPOSABLE CONTAINERS

K Number: K931664 · Decision May 23, 1994
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
112
Applicant Total
12
Review Days
413

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
SHARPS DISPOSABLE CONTAINERS
K Number
K931664
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bemis Mfg. Co.
Date Received
April 5, 1993
Decision Date
May 23, 1994
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 Bemis Mfg. Co.

K Number Device Name
K020921 NO-POKES NEEDLE SAFETY DEVICE
K965248 BEMIS TWO GALLON SHARPS CONTAINER
K964858 BEMIS TWO GALLON CHEMOTHERAPY CONTAINER
K960525 BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)
K953797 SHARPS DISPOSAL CONTAINERS
K950340 IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERS
K941665 SHARPS DISPOSAL CONTAINER/PHLEBOTOMY
K941664 SHARP DISPOSAL CONTAINERS WALL SAFE
K914601 SUCTION CONNECTING TUBING
K911576 CHEMOTHERAPY CONTAINER
Search all 12 clearances from Bemis Mfg. Co. →