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

PIPET CALIBRATION KIT

K Number: K800062 · Decision Feb 11, 1980
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
129
Applicant Total
70
Review Days
31

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Basic Information

Device Name
PIPET CALIBRATION KIT
K Number
K800062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Streck Laboratories, Inc.
Date Received
January 11, 1980
Decision Date
February 11, 1980
Product Code
JIS
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
JIS Calibrator, Primary

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Other Clearances by Streck Laboratories, Inc.

K Number Device Name
K042587 RETIC-CHEX FOR CELL-DYN
K040107 CYTO-CHEX BCT
K040025 A1C-CELLULAR
K023656 SICKLE-CHEX SOLUBILITY KIT
K021922 MODIFICATION TO PARA 5X
K020469 CAL-CHEX CD PLUS
K013316 SICKLE-CHEX
K011410 PARA 5X
K001443 SUGAR CHEX ONE
K000945 PARA 12 PLUS RETICS
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