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

BAG DECANTER

K Number: K852777 · Decision Aug 16, 1985
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
32
Review Days
46

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
BAG DECANTER
K Number
K852777
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Advance Medical Designs, Inc.
Date Received
July 1, 1985
Decision Date
August 16, 1985
Product Code
KPE
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
KPE Container, I.V.

Similar 510(k) Clearances

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

View all

Other Clearances by Advance Medical Designs, Inc.

K Number Device Name
K223689 Disposable Needle Guides and Grids
K163050 Advance Medical Designs, Inc. Sterile Ultrasound Gel
K053495 EQUIPMENT SLUSH DRAPE
K011265 ULTRASOUND TRANSDUCER COVER
K012168 ADVANCE MEDICAL DESIGNS FLUID POUCH
K011422 SURGICAL DRAPES
K003670 PATIENT DRAPE, SURGICAL
K911884 ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES
K925115 AMD DENTIST AND HYGIENIST KITS
K915301 ADVANCE STOPCOCK/HIGH PRESSURE STOPCOCK
Search all 32 clearances from Advance Medical Designs, Inc. →