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FDA 510(k)

REMA SHAVER BLADES

K-Number: K060172 · 2006-05-31

Decision Date2006-05-31
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REMA SHAVER BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Rema Medizintechnik GmbH.. It received FDA 510(k) clearance on 2006-05-31 under 510(k) number K060172. 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 REMA SHAVER BLADES?

REMA SHAVER BLADES is a medical device that received FDA 510(k) clearance on 2006-05-31. The listed applicant is Rema Medizintechnik GmbH.. The 510(k) number is K060172.

When did REMA SHAVER BLADES receive FDA 510(k) clearance?

REMA SHAVER BLADES received FDA 510(k) clearance on 2006-05-31, under 510(k) number K060172.

Who is the listed applicant for REMA SHAVER BLADES?

The FDA 510(k) record lists Rema Medizintechnik GmbH. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REMA SHAVER BLADES?

The FDA product code for REMA 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.

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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