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

COATRON F(SAME AS COATRON, BUT ALSO DOES FIBRINOGE

K Number: K851153 · Decision Nov 5, 1985
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
4
Review Days
228

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Basic Information

Device Name
COATRON F(SAME AS COATRON, BUT ALSO DOES FIBRINOGE
K Number
K851153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Astral Medical Systems
Date Received
March 22, 1985
Decision Date
November 5, 1985
Product Code
JPA
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
JPA System, Multipurpose For In Vitro Coagulation Studies

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JPA), ordered by most recent decision date.

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Other Clearances by Astral Medical Systems

K Number Device Name
K900506 MODIFIED COATRON II AND COATRON JR.
K853734 APOLLO DENSITOMETER
K851154 ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18