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FDA 510(k)

FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01

K-Number: K940085 · 1994-12-07

ApplicantSense Technology, Inc.
Decision Date1994-12-07
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01 is the device name listed in this FDA 510(k) record. The listed applicant is Sense Technology, Inc.. It received FDA 510(k) clearance on 1994-12-07 under 510(k) number K940085. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01?

FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01 is a medical device that received FDA 510(k) clearance on 1994-12-07. The listed applicant is Sense Technology, Inc.. The 510(k) number is K940085.

When did FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01 receive FDA 510(k) clearance?

FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01 received FDA 510(k) clearance on 1994-12-07, under 510(k) number K940085.

Who is the listed applicant for FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01?

The FDA 510(k) record lists Sense Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01?

The FDA product code for FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01 is LXM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Sense Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K973914SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR

Related Devices (Code: LXM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K172536Atlas Percussion Adjusting InstrumentSpinalight, Inc.K160278VSTAAR AdjusteRSpinal Acoustics, LLCK112606ACTIVATOR V-EActivator Methods International, Ltd.K082218MAX ADJUSTING INSTRUMENTManna Omni International, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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