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FDA 510(k)

PEAK FLOW METER MINIMAX

K-Number: K980443 · 1998-04-30

ApplicantThe D&T, Inc.
Decision Date1998-04-30
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEAK FLOW METER MINIMAX is the device name listed in this FDA 510(k) record. The listed applicant is The D&T, Inc.. It received FDA 510(k) clearance on 1998-04-30 under 510(k) number K980443. 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 PEAK FLOW METER MINIMAX?

PEAK FLOW METER MINIMAX is a medical device that received FDA 510(k) clearance on 1998-04-30. The listed applicant is The D&T, Inc.. The 510(k) number is K980443.

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

PEAK FLOW METER MINIMAX received FDA 510(k) clearance on 1998-04-30, under 510(k) number K980443.

Who is the listed applicant for PEAK FLOW METER MINIMAX?

The FDA 510(k) record lists The D&T, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

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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.

K253180Microlife Digital Peak Flow Meter, Model PF200B (PF200B)Microlife CorporationK252802Peak Flow Meter (PF-10(BR-PEF231))Shenzhen Bi-Rich Medical Devices Co., Ltd.K241338Peak Flow MeterChongqing Moffy Innovation Technology Co., Ltd.K232588Aluna 2Knox Medical DiagnosticsK230423Electronic Peak Flow MeterTaian Dalu Medical Instrument Co., Ltd.K222810TD-7301 Peak Flow meterGostar Co., Ltd.

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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