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

TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS

K Number: K071445 · Decision Oct 29, 2007
Classifications
1
FEI Numbers
462
Registration Numbers
462
Same Product Code
228
Applicant Total
4
Review Days
158

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Basic Information

Device Name
TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS
K Number
K071445
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Escada International, Inc.
Date Received
May 24, 2007
Decision Date
October 29, 2007
Product Code
ILY
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ILY Lamp, Infrared, Therapeutic Heating

Similar 510(k) Clearances

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

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Other Clearances by Escada International, Inc.

K Number Device Name
K080102 TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM
K061614 TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS
K043055 TERRAQUANT MQ2000 LASER THERAPY DEVICE