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FDA 510(k)

INSPIRATORY FORCE ADAPTOR

K-Number: K771518 · 1977-08-16

ApplicantVital Flow Products Corp.
Decision Date1977-08-16
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRATORY FORCE ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Vital Flow Products Corp.. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771518. 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 INSPIRATORY FORCE ADAPTOR?

INSPIRATORY FORCE ADAPTOR is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is Vital Flow Products Corp.. The 510(k) number is K771518.

When did INSPIRATORY FORCE ADAPTOR receive FDA 510(k) clearance?

INSPIRATORY FORCE ADAPTOR received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771518.

Who is the listed applicant for INSPIRATORY FORCE ADAPTOR?

The FDA 510(k) record lists Vital Flow Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSPIRATORY FORCE ADAPTOR?

The FDA product code for INSPIRATORY FORCE ADAPTOR is CAI.

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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

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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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