FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

MYOLEX

K Number: K863730 · Decision Oct 15, 1986
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
45
Applicant Total
21
Review Days
22

Basic Information

Device Name
MYOLEX
K Number
K863730
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5680
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
ORION CORP.
Date Received
September 23, 1986
Decision Date
October 15, 1986
Product Code
DDR
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DDR Myoglobin, Antigen, Antiserum, Control

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Other Clearances by ORION CORP.

K Number Device Name
K912391 RUBALEX, MODIFICATION
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K884650 RESUBMITTED SCANORA
K890199 DENTOCULT SM-STRIP MUTANS
K881505 MAMEX DC MG11
K881506 MAMEX DC MAG MG12
K874040 MAMEX DC S SL10/MG14
K872744 MODIFIED CHLAMYSET ANTIGEN
K864457 CHLAMYSET ANTIBODY EIA
K872301 DENTOCULT-SM CULTURE-PADDLE
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