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FDA 510(k)

STORZ RANEY SCALP CLIP, MODEL 1-20-004-05

K-Number: K033660 · 2004-01-07

ApplicantRudolf Storz GmbH
Decision Date2004-01-07
Product CodeHBO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STORZ RANEY SCALP CLIP, MODEL 1-20-004-05 is the device name listed in this FDA 510(k) record. The listed applicant is Rudolf Storz GmbH. It received FDA 510(k) clearance on 2004-01-07 under 510(k) number K033660. The device is classified under product code HBO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ RANEY SCALP CLIP, MODEL 1-20-004-05?

STORZ RANEY SCALP CLIP, MODEL 1-20-004-05 is a medical device that received FDA 510(k) clearance on 2004-01-07. The listed applicant is Rudolf Storz GmbH. The 510(k) number is K033660.

When did STORZ RANEY SCALP CLIP, MODEL 1-20-004-05 receive FDA 510(k) clearance?

STORZ RANEY SCALP CLIP, MODEL 1-20-004-05 received FDA 510(k) clearance on 2004-01-07, under 510(k) number K033660.

Who is the listed applicant for STORZ RANEY SCALP CLIP, MODEL 1-20-004-05?

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

What is the FDA product code for STORZ RANEY SCALP CLIP, MODEL 1-20-004-05?

The FDA product code for STORZ RANEY SCALP CLIP, MODEL 1-20-004-05 is HBO.

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Related Devices (Code: HBO)

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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