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FDA 510(k)

STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN

K-Number: K933424 · 1993-09-20

ApplicantZyloware Corp.
Decision Date1993-09-20
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN is the device name listed in this FDA 510(k) record. The listed applicant is Zyloware Corp.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K933424. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN?

STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Zyloware Corp.. The 510(k) number is K933424.

When did STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN receive FDA 510(k) clearance?

STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN received FDA 510(k) clearance on 1993-09-20, under 510(k) number K933424.

Who is the listed applicant for STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN?

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

What is the FDA product code for STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN?

The FDA product code for STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN is HQZ.

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Related Devices (Code: HQZ)

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

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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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