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FDA 510(k)

WEE BAG O'MERCURY

K-Number: K840004 · 1984-03-22

ApplicantSurgi-Quip Inc.U
Decision Date1984-03-22
Product CodeLCC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WEE BAG O'MERCURY is the device name listed in this FDA 510(k) record. The listed applicant is Surgi-Quip Inc.U. It received FDA 510(k) clearance on 1984-03-22 under 510(k) number K840004. The device is classified under product code LCC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEE BAG O'MERCURY?

WEE BAG O'MERCURY is a medical device that received FDA 510(k) clearance on 1984-03-22. The listed applicant is Surgi-Quip Inc.U. The 510(k) number is K840004.

When did WEE BAG O'MERCURY receive FDA 510(k) clearance?

WEE BAG O'MERCURY received FDA 510(k) clearance on 1984-03-22, under 510(k) number K840004.

Who is the listed applicant for WEE BAG O'MERCURY?

The FDA 510(k) record lists Surgi-Quip Inc.U as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEE BAG O'MERCURY?

The FDA product code for WEE BAG O'MERCURY is LCC.

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Other records listing Surgi-Quip Inc.U 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.

K841116MOBILE OPHTHALMIC OPERATING TABLEK841115CHARLES/MCINTYRE GIANT BREAK TABLEK832887ELECTRONIC UNITK822554CEMENT EXTRACTION INSTRUMENTATIONK822427SELF-CONTAINED MOBILE OPHTHAL. OPER. .K822428SURGI-QUIP MICROSCOPE STAND

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Related Devices (Code: LCC)

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.

K112952ILWAIT TIMER OCULOPRESSOROryx Medical Pty, Ltd.K946194WEE BAG O'MERCURYMicrosurgical Technology, Inc.K852032OCULAR PRESSURE REDUCER (MCCANNEL)Visitec Co.K820526RELIEF VALVE-HONAN INTRAOC. PRESSUREThe Lebanon Corp.K792255NEVYAS AUTOPRESS EYE COMPRESSORKeeler Optical Products , Ltd.

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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