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FDA 510(k)

TRUPEAK PEAK FLOW METER

K-Number: K963095 · 1996-11-04

Decision Date1996-11-04
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRUPEAK PEAK FLOW METER is the device name listed in this FDA 510(k) record. The listed applicant is Monaghan Medical Corp.. It received FDA 510(k) clearance on 1996-11-04 under 510(k) number K963095. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRUPEAK PEAK FLOW METER?

TRUPEAK PEAK FLOW METER is a medical device that received FDA 510(k) clearance on 1996-11-04. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K963095.

When did TRUPEAK PEAK FLOW METER receive FDA 510(k) clearance?

TRUPEAK PEAK FLOW METER received FDA 510(k) clearance on 1996-11-04, under 510(k) number K963095.

Who is the listed applicant for TRUPEAK PEAK FLOW METER?

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

What is the FDA product code for TRUPEAK PEAK FLOW METER?

The FDA product code for TRUPEAK PEAK FLOW METER is BZH.

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 Monaghan Medical Corp. 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 33 devices →

Related Devices (Code: BZH)

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

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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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