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

IF-II (TM), MODEL 7200

K Number: K923914 · Decision Nov 6, 1992
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
49
Review Days
98

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
IF-II (TM), MODEL 7200
K Number
K923914
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medical Devices, Inc.
Date Received
July 31, 1992
Decision Date
November 6, 1992
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 Medical Devices, Inc.

K Number Device Name
K002280 PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602
K930084 MICRO-ARTHROSCOPE
K943126 ELECTROFLEX
K940012 SMARTBRACE ELECTRODE
K935132 HOME MICROCURRENT HMC
K934619 FLEXMATE
K924897 XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300
K930053 VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10
K920071 MEDITRON AUTOMATIC ELECTRONIC INSUFF. MODEL AEI-15
K915694 MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR
Search all 49 clearances from Medical Devices, Inc. →