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FDA 510(k)

CLEAN SCRAPE

K-Number: K003773 · 2001-02-02

ApplicantWebb Research Ii, Inc.
Decision Date2001-02-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEAN SCRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Webb Research Ii, Inc.. It received FDA 510(k) clearance on 2001-02-02 under 510(k) number K003773. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAN SCRAPE?

CLEAN SCRAPE is a medical device that received FDA 510(k) clearance on 2001-02-02. The listed applicant is Webb Research Ii, Inc.. The 510(k) number is K003773.

When did CLEAN SCRAPE receive FDA 510(k) clearance?

CLEAN SCRAPE received FDA 510(k) clearance on 2001-02-02, under 510(k) number K003773.

Who is the listed applicant for CLEAN SCRAPE?

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

What is the FDA product code for CLEAN SCRAPE?

The FDA product code for CLEAN SCRAPE is GEI.

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.

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Other records listing Webb Research Ii, 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.

K934755FAST FIND GRIND

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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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