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

TOUCH TEAR IGE MICROASSAY KIT

K Number: K991316 · Decision Aug 9, 1999
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
3
Review Days
112

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Basic Information

Device Name
TOUCH TEAR IGE MICROASSAY KIT
K Number
K991316
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Touch Scientific, Inc.
Date Received
April 19, 1999
Decision Date
August 9, 1999
Product Code
DGC
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
DGC Ige, Antigen, Antiserum, Control

Similar 510(k) Clearances

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

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Other Clearances by Touch Scientific, Inc.

K Number Device Name
K934473 LACTOFERRIN MICROASSAY SYSTEM
K931901 LACTOCARD