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

HEMACOUNT WRIGHT GIEMSA STAIN PACK

K Number: K822602 · Decision Sep 17, 1982
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
37
Applicant Total
20
Review Days
21

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Basic Information

Device Name
HEMACOUNT WRIGHT GIEMSA STAIN PACK
K Number
K822602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1540
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Accra Laboratories, Inc.
Date Received
August 27, 1982
Decision Date
September 17, 1982
Product Code
JAF
Advisory Committee
Radiology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
JAF Monitor, Ultrasonic, Nonfetal

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Other Clearances by Accra Laboratories, Inc.

K Number Device Name
K851493 KINYOUN ACID FAST STAIN KIT
K851494 TWO-STEP ACID FAST BACTERIA STAIN
K843427 GILL PAPANICOLAOU STAIN EA-1 & 2 OG-6
K843425 HARRIS HEMATOXYLIN, MERCURY FREE, ACID
K843428 BIOFIX
K843426 EOSIN Y 1% ALCOHOLIC
K843429 GRAM STAIN SET W/STABILIZED IODINE
K831090 HEMATOXYLIN GILL FORMULATION IX#56016
K830542 HEMAQUIK II STAINING SOLUTION #55961
K823329 PAPINCOLABU STAIN EA-36/50/65 & OG-6
Search all 20 clearances from Accra Laboratories, Inc. →