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

MICRO-MIX PIPETTE SHAKER

K Number: K770165 · Decision Jan 31, 1977
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
7
Applicant Total
51
Review Days
6

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Basic Information

Device Name
MICRO-MIX PIPETTE SHAKER
K Number
K770165
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Maddak, Inc.
Date Received
January 25, 1977
Decision Date
January 31, 1977
Product Code
JRQ
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
JRQ Shaker/Stirrer

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K Number Device Name
K841700 WALK & ROLL
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K841697 HYDRO-THERO PAD
K841692 PRONE STANDER
K841691 SPLIT SEAT POSITIONING CHAIR
K841693 STANDING FRAME
K834311 NIGHT TRAINER
K833870 KNEE WALKER
K833177 GLOSSECTOMY FEEDING SPOONS
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