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FDA 510(k)

WOMED NICRO-CRAFT POWER SYSTEM

K-Number: K791407 · 1979-08-22

ApplicantXomed, Inc.
Decision Date1979-08-22
Product CodeERL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

WOMED NICRO-CRAFT POWER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1979-08-22 under 510(k) number K791407. The device is classified under product code ERL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOMED NICRO-CRAFT POWER SYSTEM?

WOMED NICRO-CRAFT POWER SYSTEM is a medical device that received FDA 510(k) clearance on 1979-08-22. The listed applicant is Xomed, Inc.. The 510(k) number is K791407.

When did WOMED NICRO-CRAFT POWER SYSTEM receive FDA 510(k) clearance?

WOMED NICRO-CRAFT POWER SYSTEM received FDA 510(k) clearance on 1979-08-22, under 510(k) number K791407.

Who is the listed applicant for WOMED NICRO-CRAFT POWER SYSTEM?

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

What is the FDA product code for WOMED NICRO-CRAFT POWER SYSTEM?

The FDA product code for WOMED NICRO-CRAFT POWER SYSTEM is ERL.

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.

Other records listing Xomed, 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.

View all 82 devices →

Related Devices (Code: ERL)

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.

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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