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

LIPOGEN RHEUMELISA DSDNA ASSAY

K Number: K902636 · Decision Jun 28, 1990
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
6
Applicant Total
15
Review Days
14

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Basic Information

Device Name
LIPOGEN RHEUMELISA DSDNA ASSAY
K Number
K902636
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Lipogen, Inc.
Date Received
June 14, 1990
Decision Date
June 28, 1990
Product Code
LRY
Advisory Committee
General, Plastic Surgery
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
LRY Punch, Surgical

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Other Clearances by Lipogen, Inc.

K Number Device Name
K895997 RHEUMELISA ASSAY FOR RNP AUTOANTIBODIES
K895996 RHEUMELISA ASSAY FOR SM AUTOANTIBODIES
K895995 RHEUMELISA ASSAY FOR SS-B/LA AUTOANTIBODIES
K895994 RHEUMELISA ASSAY FOR SS-A/RO AUTOANTIBODIES
K894659 ANA ANTISERA CONTROL KIT
K892421 MODIFIED ACCESS R-CLONE ANA/RF SCREENING TEST
K885048 ACCESS R-CLONE ANA PROFILE ASSAY
K882740 ACCESS R-CLONE(TM) ANA/RF SCREENING ASSAY
K880254 SM ANTIBODY TEST KIT
K874152 RNP ANTIBODY TEST KIT
Search all 15 clearances from Lipogen, Inc. →