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FDA 510(k)

WEE BAG O'MERCURY

K-Number: K946194 · 1995-02-27

ApplicantMicrosurgical Technology, Inc.
Decision Date1995-02-27
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 Microsurgical Technology, Inc.. It received FDA 510(k) clearance on 1995-02-27 under 510(k) number K946194. 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 1995-02-27. The listed applicant is Microsurgical Technology, Inc.. The 510(k) number is K946194.

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

WEE BAG O'MERCURY received FDA 510(k) clearance on 1995-02-27, under 510(k) number K946194.

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

The FDA 510(k) record lists Microsurgical Technology, Inc. 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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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.K852032OCULAR PRESSURE REDUCER (MCCANNEL)Visitec Co.K840004WEE BAG O'MERCURYSurgi-Quip Inc.UK820526RELIEF 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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