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FDA 510(k)

VENTILATOR CIRCUITS

K-Number: K760565 · 1976-09-16

ApplicantForegger Air Products & Chem., Inc.
Decision Date1976-09-16
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTILATOR CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Foregger Air Products & Chem., Inc.. It received FDA 510(k) clearance on 1976-09-16 under 510(k) number K760565. 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 VENTILATOR CIRCUITS?

VENTILATOR CIRCUITS is a medical device that received FDA 510(k) clearance on 1976-09-16. The listed applicant is Foregger Air Products & Chem., Inc.. The 510(k) number is K760565.

When did VENTILATOR CIRCUITS receive FDA 510(k) clearance?

VENTILATOR CIRCUITS received FDA 510(k) clearance on 1976-09-16, under 510(k) number K760565.

Who is the listed applicant for VENTILATOR CIRCUITS?

The FDA 510(k) record lists Foregger Air Products & Chem., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTILATOR CIRCUITS?

The FDA product code for VENTILATOR CIRCUITS is CAI.

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 Foregger Air Products & Chem., Inc. 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.

K760566PREFILLED HUMIDIFIERK760567BACTERIA FILTER

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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