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FDA 510(k)

RETRACTORS AND SCRAPER

K-Number: K933008 · 1994-03-11

ApplicantBaxter Healthcare Corp
Decision Date1994-03-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RETRACTORS AND SCRAPER is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K933008. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RETRACTORS AND SCRAPER?

RETRACTORS AND SCRAPER is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K933008.

When did RETRACTORS AND SCRAPER receive FDA 510(k) clearance?

RETRACTORS AND SCRAPER received FDA 510(k) clearance on 1994-03-11, under 510(k) number K933008.

Who is the listed applicant for RETRACTORS AND SCRAPER?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RETRACTORS AND SCRAPER?

The FDA product code for RETRACTORS AND SCRAPER is HET.

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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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