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

POLYPET

K Number: K860617 · Decision Mar 3, 1986
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
65
Applicant Total
7
Review Days
12

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Basic Information

Device Name
POLYPET
K Number
K860617
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2500
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Instrumed, Inc.
Date Received
February 19, 1986
Decision Date
March 3, 1986
Product Code
JTC
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
JTC Device, Microtiter Diluting/Dispensing

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Other Clearances by Instrumed, Inc.

K Number Device Name
K952038 CLEAN-CUFF
K940615 ACCUTEST
K924273 ACCUFLATE
K924373 ACCUFLATE ACCESSORIE CART W/IV POLE AND CLAMP
K910512 ACCUFLATE
K890014 DISPOSABLE COLOR-CUFFS