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

THERMOPULS E

K Number: K844416 · Decision Mar 12, 1985
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
44
Applicant Total
13
Review Days
118

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
THERMOPULS E
K Number
K844416
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5290
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Nemectron Medical, Inc.
Date Received
November 14, 1984
Decision Date
March 12, 1985
Product Code
IMJ
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
IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

Similar 510(k) Clearances

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

View all

Other Clearances by Nemectron Medical, Inc.

K Number Device Name
K923396 THERMODYN
K895000 NEMECTRON MICROWAVE
K862376 NEMECTROSON MODEL 2
K854720 NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.
K854721 NEMECTRODYN MODEL 2 & ENDOVAC 2
K843735 SOFTEPIL
K843734 NEMDI
K823511 EMG BIOFEEDBACK DEVICE
K820334 NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV
K810513 ELECTRODYN CII-INTERFERENTIAL MUSCLE
Search all 13 clearances from Nemectron Medical, Inc. →