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FDA 510(k)

FORCE SENSING ARRAY

K-Number: K924705 · 1993-05-12

ApplicantForce Sensing Systems
Decision Date1993-05-12
Product CodeJFC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORCE SENSING ARRAY is the device name listed in this FDA 510(k) record. The listed applicant is Force Sensing Systems. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K924705. The device is classified under product code JFC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCE SENSING ARRAY?

FORCE SENSING ARRAY is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is Force Sensing Systems. The 510(k) number is K924705.

When did FORCE SENSING ARRAY receive FDA 510(k) clearance?

FORCE SENSING ARRAY received FDA 510(k) clearance on 1993-05-12, under 510(k) number K924705.

Who is the listed applicant for FORCE SENSING ARRAY?

The FDA 510(k) record lists Force Sensing Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCE SENSING ARRAY?

The FDA product code for FORCE SENSING ARRAY is JFC.

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Related Devices (Code: JFC)

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.

K925258DYNAMIC PRESSURE MONITOR 2000M AND 2000CPin Dot Products, Inc.K925052QA PRESSURE MEASUREMENT SYSTEMGabel Medical Instruments, Ltd.K915278CDG GAIT ANALYSES SYSTEMWrm ComputersK914776OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITORTalley Group, Ltd.K913510MECHANICAL SHAPE SENSORPin Dot Products, Inc.K881284COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINENathaniel Gould Diagnostics, Inc.

Official Source

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

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