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

ANHYDRIC INCUBATORS, CULTURE INCUBATOR

K Number: K831592 · Decision Jun 16, 1983
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
11
Applicant Total
3
Review Days
30

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Basic Information

Device Name
ANHYDRIC INCUBATORS, CULTURE INCUBATOR
K Number
K831592
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2540
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Boekel Industries, Inc.
Date Received
May 17, 1983
Decision Date
June 16, 1983
Product Code
JTQ
Advisory Committee
Microbiology
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
JTQ Bath, Incubators/Water, All

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Other Clearances by Boekel Industries, Inc.

K Number Device Name
K823766 BLOOD GAS INCUBATOR #260650
K822564 WATER BATH