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FDA 510(k)

PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM

K-Number: K932709 · 1993-07-23

Decision Date1993-07-23
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Precision Med Products, Ltd.. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K932709. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM?

PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Precision Med Products, Ltd.. The 510(k) number is K932709.

When did PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM receive FDA 510(k) clearance?

PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM received FDA 510(k) clearance on 1993-07-23, under 510(k) number K932709.

Who is the listed applicant for PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM?

The FDA 510(k) record lists Precision Med Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM?

The FDA product code for PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM is BZR.

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 Precision Med Products, 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.

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Related Devices (Code: BZR)

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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