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FDA 510(k)

TRANSFLOW TEST

K-Number: K953990 · 1996-12-09

ApplicantP.K. Morgan , Ltd.
Decision Date1996-12-09
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRANSFLOW TEST 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 1996-12-09 under 510(k) number K953990. 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 TRANSFLOW TEST?

TRANSFLOW TEST is a medical device that received FDA 510(k) clearance on 1996-12-09. The listed applicant is P.K. Morgan , Ltd.. The 510(k) number is K953990.

When did TRANSFLOW TEST receive FDA 510(k) clearance?

TRANSFLOW TEST received FDA 510(k) clearance on 1996-12-09, under 510(k) number K953990.

Who is the listed applicant for TRANSFLOW TEST?

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 TRANSFLOW TEST?

The FDA product code for TRANSFLOW TEST is BZC.

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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 TESTK960121AUTOLINK BODY PLETHYSMOGRAPHK954731OXYLOG 2

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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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