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FDA 510(k)

KT-1000 DEVICE

K-Number: K812806 · 1981-11-10

ApplicantMedmetric Corp.
Decision Date1981-11-10
Product CodeLYH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KT-1000 DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medmetric Corp.. It received FDA 510(k) clearance on 1981-11-10 under 510(k) number K812806. The device is classified under product code LYH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KT-1000 DEVICE?

KT-1000 DEVICE is a medical device that received FDA 510(k) clearance on 1981-11-10. The listed applicant is Medmetric Corp.. The 510(k) number is K812806.

When did KT-1000 DEVICE receive FDA 510(k) clearance?

KT-1000 DEVICE received FDA 510(k) clearance on 1981-11-10, under 510(k) number K812806.

Who is the listed applicant for KT-1000 DEVICE?

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

What is the FDA product code for KT-1000 DEVICE?

The FDA product code for KT-1000 DEVICE is LYH.

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 Medmetric Corp. 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.

K943197KT1000/S KNEE LIGAMENT ARTHROMETERK942059KT2000 KNEE LIGAMENT ARTHROMETERK904823FLEXERCYCLEK904898TORQUE FRAME QTF1000K854254TENSION-ISOMETERK812713DRAWER TEST

View all 8 devices →

Related Devices (Code: LYH)

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.

K943197KT1000/S KNEE LIGAMENT ARTHROMETERMedmetric Corp.K942059KT2000 KNEE LIGAMENT ARTHROMETERMedmetric Corp.K881876DYNAMIC CRUCIATE TESTERDyonics, Inc.K834462GENUCOMFar Orthopedics, 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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