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FDA 510(k)

MODEL 295 ELECTRONIC RESPIROMETER

K-Number: K903674 · 1991-01-04

ApplicantNational Medical Sales, Inc.
Decision Date1991-01-04
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 295 ELECTRONIC RESPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Sales, Inc.. It received FDA 510(k) clearance on 1991-01-04 under 510(k) number K903674. The device is classified under product code BZK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 295 ELECTRONIC RESPIROMETER?

MODEL 295 ELECTRONIC RESPIROMETER is a medical device that received FDA 510(k) clearance on 1991-01-04. The listed applicant is National Medical Sales, Inc.. The 510(k) number is K903674.

When did MODEL 295 ELECTRONIC RESPIROMETER receive FDA 510(k) clearance?

MODEL 295 ELECTRONIC RESPIROMETER received FDA 510(k) clearance on 1991-01-04, under 510(k) number K903674.

Who is the listed applicant for MODEL 295 ELECTRONIC RESPIROMETER?

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

What is the FDA product code for MODEL 295 ELECTRONIC RESPIROMETER?

The FDA product code for MODEL 295 ELECTRONIC RESPIROMETER is BZK.

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.

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Other records listing National Medical Sales, Inc. 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.

K861935MODEL 100 NERVE STIMULATOR

Related Devices (Code: BZK)

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.

K260226ElintMAX Respiratory Monitor (ElintMAX Monitor A1)Amptron Medical, Inc.K192584BEACON Caresystem Model 00002144Mermaid Care A/SK192595ExSpiron 2XiRespiratory MotionK180788Gas Module 3Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K173181ExSpiron 1XiRespiratory Motion, Inc.K162131ExSpiron 1XiRespiratory Motion, Inc.

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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