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FDA 510(k)

LARGE VOLUME FLUID RESERVOIR

K-Number: K032778 · 2003-09-22

ApplicantBelmont Instrument Corp.
Decision Date2003-09-22
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LARGE VOLUME FLUID RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Belmont Instrument Corp.. It received FDA 510(k) clearance on 2003-09-22 under 510(k) number K032778. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARGE VOLUME FLUID RESERVOIR?

LARGE VOLUME FLUID RESERVOIR is a medical device that received FDA 510(k) clearance on 2003-09-22. The listed applicant is Belmont Instrument Corp.. The 510(k) number is K032778.

When did LARGE VOLUME FLUID RESERVOIR receive FDA 510(k) clearance?

LARGE VOLUME FLUID RESERVOIR received FDA 510(k) clearance on 2003-09-22, under 510(k) number K032778.

Who is the listed applicant for LARGE VOLUME FLUID RESERVOIR?

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

What is the FDA product code for LARGE VOLUME FLUID RESERVOIR?

The FDA product code for LARGE VOLUME FLUID RESERVOIR is LGZ.

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Other records listing Belmont Instrument Corp. as applicant

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Related Devices (Code: LGZ)

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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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