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FDA 510(k)

ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP

K-Number: K893919 · 1989-09-15

ApplicantBaxter Healthcare Corp
Decision Date1989-09-15
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1989-09-15 under 510(k) number K893919. 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 ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP?

ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP is a medical device that received FDA 510(k) clearance on 1989-09-15. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K893919.

When did ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP receive FDA 510(k) clearance?

ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP received FDA 510(k) clearance on 1989-09-15, under 510(k) number K893919.

Who is the listed applicant for ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP?

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

What is the FDA product code for ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP?

The FDA product code for ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP is CAI.

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Other records listing Baxter Healthcare Corp as applicant

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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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