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

STIMULATOR, MODEL 1-600 ELECTRIC NERVR

K Number: K782164 · Decision Mar 8, 1979
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
23
Review Days
76

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
STIMULATOR, MODEL 1-600 ELECTRIC NERVR
K Number
K782164
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Ipco Corp.
Date Received
December 22, 1978
Decision Date
March 8, 1979
Product Code
GZJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

Similar 510(k) Clearances

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

View all

Other Clearances by Ipco Corp.

K Number Device Name
K871270 PERFORM DENTURE BASE RESIN
K850666 STROBEX ULTRON ELECTROSURGE-DENTAL UNIT
K850906 TACTILE PLUS DENTAL ELEVATORS
K842836 SAFE & SOFT MINI PADS & MAXI PADS
K842837 SAFE & SOFT MAXI SHILEDS
K842838 SAFE & SOFT PANTY SHIELDS
K841953 ULTRA SHIELD BRIEFS
K840753 AMBEZE DISPOSABLE INCONTINENCE PANTS
K840754 MAXISHIELD INCONTINENCE CARE SYSTEM
K840755 MINIGARD DISPOSABLE LINERS
Search all 23 clearances from Ipco Corp. →