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FDA 510(k)

SPARROWHAWK DISPOSABLE

K-Number: K010473 · 2001-06-06

ApplicantAtc Technologies, Inc.
Decision Date2001-06-06
Product CodeDWZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SPARROWHAWK DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Atc Technologies, Inc.. It received FDA 510(k) clearance on 2001-06-06 under 510(k) number K010473. The device is classified under product code DWZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPARROWHAWK DISPOSABLE?

SPARROWHAWK DISPOSABLE is a medical device that received FDA 510(k) clearance on 2001-06-06. The listed applicant is Atc Technologies, Inc.. The 510(k) number is K010473.

When did SPARROWHAWK DISPOSABLE receive FDA 510(k) clearance?

SPARROWHAWK DISPOSABLE received FDA 510(k) clearance on 2001-06-06, under 510(k) number K010473.

Who is the listed applicant for SPARROWHAWK DISPOSABLE?

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

What is the FDA product code for SPARROWHAWK DISPOSABLE?

The FDA product code for SPARROWHAWK DISPOSABLE is DWZ.

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Other records listing Atc Technologies, 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.

K121343MODULAP LOOPK994319MODULAPK983623MODULAP

Related Devices (Code: DWZ)

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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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