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FDA 510(k)

PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS

K-Number: K932485 · 1993-07-13

ApplicantPrecision Med Products, Ltd.
Decision Date1993-07-13
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS 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 1993-07-13 under 510(k) number K932485. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS?

PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Precision Med Products, Ltd.. The 510(k) number is K932485.

When did PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS receive FDA 510(k) clearance?

PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS received FDA 510(k) clearance on 1993-07-13, under 510(k) number K932485.

Who is the listed applicant for PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS?

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. COAXIAL CIRCUITS?

The FDA product code for PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS is CAI.

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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: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, 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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