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FDA 510(k)

SUPER STAPLE(TM) CLASSIC

K-Number: K123363 · 2013-01-03

ApplicantMetric Medical Devices, Inc.
Decision Date2013-01-03
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SUPER STAPLE(TM) CLASSIC is the device name listed in this FDA 510(k) record. The listed applicant is Metric Medical Devices, Inc.. It received FDA 510(k) clearance on 2013-01-03 under 510(k) number K123363. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER STAPLE(TM) CLASSIC?

SUPER STAPLE(TM) CLASSIC is a medical device that received FDA 510(k) clearance on 2013-01-03. The listed applicant is Metric Medical Devices, Inc.. The 510(k) number is K123363.

When did SUPER STAPLE(TM) CLASSIC receive FDA 510(k) clearance?

SUPER STAPLE(TM) CLASSIC received FDA 510(k) clearance on 2013-01-03, under 510(k) number K123363.

Who is the listed applicant for SUPER STAPLE(TM) CLASSIC?

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

What is the FDA product code for SUPER STAPLE(TM) CLASSIC?

The FDA product code for SUPER STAPLE(TM) CLASSIC is JDR.

Related Clinical Trials

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Other records listing Metric Medical Devices, 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.

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Related Devices (Code: JDR)

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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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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