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FDA 510(k)

KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)

K-Number: K911795 · 1991-11-19

ApplicantBreg, Inc.
Decision Date1991-11-19
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000) is the device name listed in this FDA 510(k) record. The listed applicant is Breg, Inc.. It received FDA 510(k) clearance on 1991-11-19 under 510(k) number K911795. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)?

KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000) is a medical device that received FDA 510(k) clearance on 1991-11-19. The listed applicant is Breg, Inc.. The 510(k) number is K911795.

When did KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000) receive FDA 510(k) clearance?

KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000) received FDA 510(k) clearance on 1991-11-19, under 510(k) number K911795.

Who is the listed applicant for KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)?

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

What is the FDA product code for KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)?

The FDA product code for KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000) is LXV.

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Other records listing Breg, 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.

K183702Polar Care WaveK070402MODIFICATION TO POLAR CARE 500K041714E-PAIN CAREK020988PAIN CARE 4200K013928PAIN CARE 3200K003611PAIN CARE MULTI-PORT CATHETER, MODEL 2000L

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Related Devices (Code: LXV)

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.

K220231GyroStimUltrathera Technologies, Inc.K200529OrionInteracoustics A/SK192652TRVInteracoustics A/SK183661ClearEdge Balance SystemQuadrant BiosciencesK190735EQ BalanceUpright Science, Inc.K173669K-D BalanceKing-Devick Technologies, 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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