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

OMNI STIM II

K Number: K813604 · Decision Mar 8, 1982
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
12
Review Days
70

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
OMNI STIM II
K Number
K813604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Omni Intl., Inc.
Date Received
December 28, 1981
Decision Date
March 8, 1982
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Omni Intl., Inc.

K Number Device Name
K984066 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM
K984064 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE
K853255 OMNIMED I.V. SOLUTION ADMIN. SET
K851938 OMNIMED SURGICAL GOWN
K851654 OMNIMED CLAMP
K851734 OMNIMED SUPERIOR TRANSDUCER PROTECTOR
K850706 F-SERIES IMPLANT
K850112 OMNIMED IV SOLUTION ADMINISTRATION SET
K850066 OMNIMED NASAL OXYGEN CANNULA
K831147 OMNIPROBE ELECTRICAL NERVE STIMULATOR
Search all 12 clearances from Omni Intl., Inc. →