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FDA 510(k)

PACIFIC MARQUIS SPA

K-Number: K910607 · 1991-02-21

ApplicantMarquis International , Ltd.
Decision Date1991-02-21
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PACIFIC MARQUIS SPA is the device name listed in this FDA 510(k) record. The listed applicant is Marquis International , Ltd.. It received FDA 510(k) clearance on 1991-02-21 under 510(k) number K910607. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACIFIC MARQUIS SPA?

PACIFIC MARQUIS SPA is a medical device that received FDA 510(k) clearance on 1991-02-21. The listed applicant is Marquis International , Ltd.. The 510(k) number is K910607.

When did PACIFIC MARQUIS SPA receive FDA 510(k) clearance?

PACIFIC MARQUIS SPA received FDA 510(k) clearance on 1991-02-21, under 510(k) number K910607.

Who is the listed applicant for PACIFIC MARQUIS SPA?

The FDA 510(k) record lists Marquis International , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PACIFIC MARQUIS SPA?

The FDA product code for PACIFIC MARQUIS SPA is ILJ.

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Related Devices (Code: ILJ)

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.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.

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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