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FDA 510(k)

DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS

K-Number: K891479 · 1989-05-05

ApplicantAnetec, Inc.
Decision Date1989-05-05
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Anetec, Inc.. It received FDA 510(k) clearance on 1989-05-05 under 510(k) number K891479. 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 DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS?

DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS is a medical device that received FDA 510(k) clearance on 1989-05-05. The listed applicant is Anetec, Inc.. The 510(k) number is K891479.

When did DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS receive FDA 510(k) clearance?

DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS received FDA 510(k) clearance on 1989-05-05, under 510(k) number K891479.

Who is the listed applicant for DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS?

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

What is the FDA product code for DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS?

The FDA product code for DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS is CAI.

Related Clinical Trials

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Other records listing Anetec, 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.

K944189TRANSPARENT ANESTHESIA 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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