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FDA 510(k)

EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES

K-Number: K061134 · 2006-09-01

Decision Date2006-09-01
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Efs Eberle Feinwerktechnische Systeme. It received FDA 510(k) clearance on 2006-09-01 under 510(k) number K061134. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES?

EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES is a medical device that received FDA 510(k) clearance on 2006-09-01. The listed applicant is Efs Eberle Feinwerktechnische Systeme. The 510(k) number is K061134.

When did EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES receive FDA 510(k) clearance?

EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES received FDA 510(k) clearance on 2006-09-01, under 510(k) number K061134.

Who is the listed applicant for EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES?

The FDA 510(k) record lists Efs Eberle Feinwerktechnische Systeme as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES?

The FDA product code for EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES is HRX.

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 Efs Eberle Feinwerktechnische Systeme 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.

Related Devices (Code: HRX)

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

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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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