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

BIOFIX

K Number: K843428 · Decision Sep 27, 1984
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
7
Applicant Total
20
Review Days
23

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Basic Information

Device Name
BIOFIX
K Number
K843428
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Accra Laboratories, Inc.
Date Received
September 4, 1984
Decision Date
September 27, 1984
Product Code
LDZ
Advisory Committee
Pathology
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
LDZ Fixative, Alcohol Containing

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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
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
K823328 HARRIS HEMATOXYLIN
Search all 20 clearances from Accra Laboratories, Inc. →