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FDA 510(k)

MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149

K-Number: K001714 · 2000-11-03

Decision Date2000-11-03
Product CodeNHK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149 is the device name listed in this FDA 510(k) record. The listed applicant is Mercury Medical. It received FDA 510(k) clearance on 2000-11-03 under 510(k) number K001714. The device is classified under product code NHK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149?

MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149 is a medical device that received FDA 510(k) clearance on 2000-11-03. The listed applicant is Mercury Medical. The 510(k) number is K001714.

When did MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149 receive FDA 510(k) clearance?

MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149 received FDA 510(k) clearance on 2000-11-03, under 510(k) number K001714.

Who is the listed applicant for MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149?

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

What is the FDA product code for MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149?

The FDA product code for MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149 is NHK.

Related Clinical Trials

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.

Other records listing Mercury Medical 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.

View all 14 devices →

Related Devices (Code: NHK)

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.

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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