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

MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE

K Number: K963704 · Decision Nov 26, 1996
Classifications
1
FEI Numbers
176
Registration Numbers
176
Same Product Code
12
Applicant Total
13
Review Days
71

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Basic Information

Device Name
MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE
K Number
K963704
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5660
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shippert Medical Technologies Corp.
Date Received
September 16, 1996
Decision Date
November 26, 1996
Product Code
LYG
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
LYG Massager, Therapeutic, Manual

Similar 510(k) Clearances

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Other Clearances by Shippert Medical Technologies Corp.

K Number Device Name
K102117 TISSU TRANS FILTRON SYRINGE FILL
K092482 TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500
K092022 TISSU TRANS HARVEST TUBING
K050797 TISSU-TRANS
K964855 EXPANDACELL EYE SPEAR, EYE WICK, WICK DRAIN AND CORNEAL SHIELD
K964334 EXPANDACELL ANTI-FOG INSTRUMENT WIPE (WITH ALCOHOL)/(WITHOUT)
K962133 EXPANDACELL INJECTO-PAK
K960621 EXPANDACELL INSTRUMENT WIPE
K960228 EXPANDACELL INJECTO-PAK NASAL PACK
K955593 EXPANDACELL ANATOMICAL POSTERIOR NASAL PACK W/& WITHOUT AIRWAY
Search all 13 clearances from Shippert Medical Technologies Corp. →