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

BTL-785MJ

K Number: K243290 · Decision May 9, 2025
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
8
Applicant Total
42
Review Days
203

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BTL-785MJ
K Number
K243290
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BTL Industries, Inc.
Date Received
October 18, 2024
Decision Date
May 9, 2025
Product Code
NUW
Advisory Committee
Physical Medicine
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NUW Stimulator, Muscle, Powered, Dental

Similar 510(k) Clearances

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

View all

Other Clearances by BTL Industries, Inc.

K Number Device Name
K252963 BTL-899TT
K253750 BTL-785NEH
K252561 BTL-754FF
K250309 BTL-199
K241516 BTL-398
K241270 BTL-754
K242532 BTL-785BNF-E
K240234 BTL-899MS
K233849 BTL-499
K233604 BTL-785S
Search all 42 clearances from BTL Industries, Inc. →