FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01

K Number: K940085 · Decision Dec 7, 1994
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
31
Applicant Total
2
Review Days
334

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Basic Information

Device Name
FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01
K Number
K940085
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sense Technology, Inc.
Date Received
January 7, 1994
Decision Date
December 7, 1994
Product Code
LXM
Advisory Committee
Unknown
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
LXM Manipulator, Plunger-Like Joint

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Other Clearances by Sense Technology, Inc.

K Number Device Name
K973914 SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR