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FDA 510(k)

AUTOLINK BODY PLETHYSMOGRAPH

K-Number: K960121 · 1997-01-09

ApplicantP.K. Morgan , Ltd.
Decision Date1997-01-09
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOLINK BODY PLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is P.K. Morgan , Ltd.. It received FDA 510(k) clearance on 1997-01-09 under 510(k) number K960121. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOLINK BODY PLETHYSMOGRAPH?

AUTOLINK BODY PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1997-01-09. The listed applicant is P.K. Morgan , Ltd.. The 510(k) number is K960121.

When did AUTOLINK BODY PLETHYSMOGRAPH receive FDA 510(k) clearance?

AUTOLINK BODY PLETHYSMOGRAPH received FDA 510(k) clearance on 1997-01-09, under 510(k) number K960121.

Who is the listed applicant for AUTOLINK BODY PLETHYSMOGRAPH?

The FDA 510(k) record lists P.K. Morgan , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOLINK BODY PLETHYSMOGRAPH?

The FDA product code for AUTOLINK BODY PLETHYSMOGRAPH is BZC.

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 P.K. Morgan , Ltd. 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.

K954730BENCHMARK TRANSFER TESTK954731OXYLOG 2K953990TRANSFLOW TEST

Related Devices (Code: BZC)

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.

K240293STSTechbopulm, Ltd.K183567Vyntus/SentrySuite Product LineVyaire MedicalK190853Vyntus BODYVyaire Medical, Inc.K181524Vyntus ONE with CART, Vyntus ONE PFT only with CART, Vyntus ONE with adjustable CART, Vyntus ONE PFT only with adjustable CARTVyaire Medical, Inc.K162515COSMED K5 Wearable Metabolic TechnologyCosmed SrlK161295MiniBox +Pulmone Advanced Medical Devices, Ltd.

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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