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

BTL-4000

K Number: K150353 · Decision Nov 13, 2015
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
54
Applicant Total
42
Review Days
275

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Basic Information

Device Name
BTL-4000
K Number
K150353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BTL Industries, Inc.
Date Received
February 11, 2015
Decision Date
November 13, 2015
Product Code
IMG
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
IMG Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat

Similar 510(k) Clearances

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Other Clearances by BTL Industries, Inc.

K Number Device Name
K252963 BTL-899TT
K253750 BTL-785NEH
K252561 BTL-754FF
K250309 BTL-199
K243290 BTL-785MJ
K241516 BTL-398
K241270 BTL-754
K242532 BTL-785BNF-E
K240234 BTL-899MS
K233849 BTL-499
Search all 42 clearances from BTL Industries, Inc. →