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

THERA-CREAM, MODEL TCT004

K Number: K032239 · Decision Jul 30, 2004
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
68
Applicant Total
8
Review Days
375

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Basic Information

Device Name
THERA-CREAM, MODEL TCT004
K Number
K032239
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1275
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Prizm Medical, Inc.
Date Received
July 21, 2003
Decision Date
July 30, 2004
Product Code
GYB
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GYB Media, Electroconductive

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Other Clearances by Prizm Medical, Inc.

K Number Device Name
K133502 5000Z FIREFLY SYSTEM
K033122 5000Z SYSTEM (OTC)
K024181 PRIZM MEDICAL, INC. MICRO-Z STIMULATION SYSTEM
K012974 PRIZM MEDICAL INC. THERMOTRACE INFRARED THERMOMETER MODELS 15004 AND 15007
K951727 Z-WATCH SYSTEM
K944487 ELECTRO-MESH SOCK, WRAP, AND SLEEVE ELECTRODES
K932299 ELECTRO-MESH