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

PAT PLATELET AGGREGATION TEST

K Number: K881829 · Decision Jul 1, 1988
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
11
Applicant Total
70
Review Days
63

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Basic Information

Device Name
PAT PLATELET AGGREGATION TEST
K Number
K881829
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6675
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Streck Laboratories, Inc.
Date Received
April 29, 1988
Decision Date
July 1, 1988
Product Code
JBX
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
JBX Aggregrometer, Platelet

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K021922 MODIFICATION TO PARA 5X
K020469 CAL-CHEX CD PLUS
K013316 SICKLE-CHEX
K011410 PARA 5X
K001443 SUGAR CHEX ONE
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