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FDA 510(k)

KHI CPRAM BREATHING CIRCUIT

K-Number: K811858 · 1981-07-16

ApplicantKhi, Inc.
Decision Date1981-07-16
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KHI CPRAM BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Khi, Inc.. It received FDA 510(k) clearance on 1981-07-16 under 510(k) number K811858. 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 KHI CPRAM BREATHING CIRCUIT?

KHI CPRAM BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1981-07-16. The listed applicant is Khi, Inc.. The 510(k) number is K811858.

When did KHI CPRAM BREATHING CIRCUIT receive FDA 510(k) clearance?

KHI CPRAM BREATHING CIRCUIT received FDA 510(k) clearance on 1981-07-16, under 510(k) number K811858.

Who is the listed applicant for KHI CPRAM BREATHING CIRCUIT?

The FDA 510(k) record lists Khi, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KHI CPRAM BREATHING CIRCUIT?

The FDA product code for KHI CPRAM BREATHING CIRCUIT 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 Khi, 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.

K830404RAD VALVEK830399COUPLING/VALVEK800456EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.

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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