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

CHANGING METHOD OF STERILITY RELEASE

K Number: K832368 · Decision Oct 31, 1983
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
20
Applicant Total
47
Review Days
105

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
CHANGING METHOD OF STERILITY RELEASE
K Number
K832368
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Devon Industries, Inc.
Date Received
July 18, 1983
Decision Date
October 31, 1983
Product Code
EMF
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
EMF Knife, Surgical

Similar 510(k) Clearances

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

View all

Other Clearances by Devon Industries, Inc.

K Number Device Name
K961993 BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)
K954015 ABG POINT LOK NEEDLE PROTECTION DEVICE
K946289 DEVONS POINT LOK NEEDLE PROTECTION DEVICE
K945197 THE SHARPS COLLECTION AND DISPOSAL SYSTEM
K943892 POINT OF USE SHARPS A GATOR
K944114 PHLEBOTOMY UNIT SHARPS A GATOR
K945485 ABG NEEDLE PROTECTION
K932998 EASY-ON
K912824 DEVON SPONGE COUNTER BAGS
K894170 DEVON DISPOSABLE HEAD POSITIONER COVER
Search all 47 clearances from Devon Industries, Inc. →