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

PIASTRINIT

K Number: K863114 · Decision Nov 6, 1986
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
28
Applicant Total
34
Review Days
85

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Basic Information

Device Name
PIASTRINIT
K Number
K863114
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.8540
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
J. D. Assoc.
Date Received
August 13, 1986
Decision Date
November 6, 1986
Product Code
GGK
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
GGK Products, Red-Cell Lysing Products

Similar 510(k) Clearances

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

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Other Clearances by J. D. Assoc.

K Number Device Name
K863103 PEG 6,000
K863054 AST S.C.E. (GOT)
K863069 MAGNESIOMETER
K863079 CREATINKINETIC
K863112 PROTEINMETER
K863068 LDH S.C.E.
K863053 ALT S.C.E. (GPT)
K863066 TRANSFERMETER
K863109 FERROFAST
K863102 GLUCOMETER-E
Search all 34 clearances from J. D. Assoc. →