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FDA 510(k)

DRAWER TEST

K-Number: K812713 · 1981-11-05

ApplicantMedmetric Corp.
Decision Date1981-11-05
Product CodeFTY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DRAWER TEST is the device name listed in this FDA 510(k) record. The listed applicant is Medmetric Corp.. It received FDA 510(k) clearance on 1981-11-05 under 510(k) number K812713. The device is classified under product code FTY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAWER TEST?

DRAWER TEST is a medical device that received FDA 510(k) clearance on 1981-11-05. The listed applicant is Medmetric Corp.. The 510(k) number is K812713.

When did DRAWER TEST receive FDA 510(k) clearance?

DRAWER TEST received FDA 510(k) clearance on 1981-11-05, under 510(k) number K812713.

Who is the listed applicant for DRAWER TEST?

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 DRAWER TEST?

The FDA product code for DRAWER TEST is FTY.

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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-ISOMETERK812806KT-1000 DEVICE

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Related Devices (Code: FTY)

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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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