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FDA 510(k)

EXTENSION SET, MODELS 1911-512

K-Number: K020926 · 2002-07-12

ApplicantEpimed International, Inc.
Decision Date2002-07-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXTENSION SET, MODELS 1911-512 is the device name listed in this FDA 510(k) record. The listed applicant is Epimed International, Inc.. It received FDA 510(k) clearance on 2002-07-12 under 510(k) number K020926. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENSION SET, MODELS 1911-512?

EXTENSION SET, MODELS 1911-512 is a medical device that received FDA 510(k) clearance on 2002-07-12. The listed applicant is Epimed International, Inc.. The 510(k) number is K020926.

When did EXTENSION SET, MODELS 1911-512 receive FDA 510(k) clearance?

EXTENSION SET, MODELS 1911-512 received FDA 510(k) clearance on 2002-07-12, under 510(k) number K020926.

Who is the listed applicant for EXTENSION SET, MODELS 1911-512?

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

What is the FDA product code for EXTENSION SET, MODELS 1911-512?

The FDA product code for EXTENSION SET, MODELS 1911-512 is FPA.

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Other records listing Epimed International, Inc. as applicant

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Related Devices (Code: FPA)

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

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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