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

RETIC-CHEX

K Number: K905524 · Decision Feb 20, 1991
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
70
Review Days
72

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Basic Information

Device Name
RETIC-CHEX
K Number
K905524
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Streck Laboratories, Inc.
Date Received
December 10, 1990
Decision Date
February 20, 1991
Product Code
JPK
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
JPK Mixture, Hematology Quality Control

Similar 510(k) Clearances

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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
Search all 70 clearances from Streck Laboratories, Inc. →