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FDA 510(k)

PRECISION MED PRODUCTS LTD VOLUME VENTILATORS

K-Number: K932712 · 1993-07-22

ApplicantPrecision Med Products, Ltd.
Decision Date1993-07-22
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRECISION MED PRODUCTS LTD VOLUME VENTILATORS 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 1993-07-22 under 510(k) number K932712. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION MED PRODUCTS LTD VOLUME VENTILATORS?

PRECISION MED PRODUCTS LTD VOLUME VENTILATORS is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Precision Med Products, Ltd.. The 510(k) number is K932712.

When did PRECISION MED PRODUCTS LTD VOLUME VENTILATORS receive FDA 510(k) clearance?

PRECISION MED PRODUCTS LTD VOLUME VENTILATORS received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932712.

Who is the listed applicant for PRECISION MED PRODUCTS LTD VOLUME VENTILATORS?

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 VOLUME VENTILATORS?

The FDA product code for PRECISION MED PRODUCTS LTD VOLUME VENTILATORS is BZO.

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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.

K932710GAS SAMPLING LINES AND CONNECTORSK932709PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEMK932707ADULT ANESTHESIA BREATHING CIRCUITK932708PRECISION MED PRODUCTS LTD MAPLESON D CIRCUITSK932711PRECISION MED PRODUCTS LTD GUEDEL AIRWAYSK932706PRECISION MED PRODUCTS LTD. VENTILATOR HOSE

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Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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