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

GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER

K Number: K850260 · Decision Feb 27, 1985
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
17
Applicant Total
32
Review Days
36

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
GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER
K Number
K850260
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2400
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Gelman Sciences, Inc.
Date Received
January 22, 1985
Decision Date
February 27, 1985
Product Code
JQT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JQT Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica

Similar 510(k) Clearances

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

View all

Other Clearances by Gelman Sciences, Inc.

K Number Device Name
K946190 DRUG DISPENSING SPIKE
K943127 PHARMASSURE LARGE VOLUME TRANSFER FILTERS
K941589 SYRINGE FILTER DEVICES
K941020 DRUG RECONSTITUTION FILTER DEVICE
K942275 VIAL VENT FILTER
K941032 UNKNOWN
K910821 TRANSDUCER PROTECTOR
K892387 MODIFIED GELMAN ARTERIAL FILTER
K884176 CHROMATOGRAPHY KIT
K884178 DRUG CONTROL SET
Search all 32 clearances from Gelman Sciences, Inc. →