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FDA 510(k)

ZEFON ADULT ANESTHESIA BREATHING CIRCUIT

K-Number: K924889 · 1993-03-19

ApplicantZefon Medical Products
Decision Date1993-03-19
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ZEFON ADULT ANESTHESIA BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Zefon Medical Products. It received FDA 510(k) clearance on 1993-03-19 under 510(k) number K924889. 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 ZEFON ADULT ANESTHESIA BREATHING CIRCUIT?

ZEFON ADULT ANESTHESIA BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1993-03-19. The listed applicant is Zefon Medical Products. The 510(k) number is K924889.

When did ZEFON ADULT ANESTHESIA BREATHING CIRCUIT receive FDA 510(k) clearance?

ZEFON ADULT ANESTHESIA BREATHING CIRCUIT received FDA 510(k) clearance on 1993-03-19, under 510(k) number K924889.

Who is the listed applicant for ZEFON ADULT ANESTHESIA BREATHING CIRCUIT?

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

What is the FDA product code for ZEFON ADULT ANESTHESIA BREATHING CIRCUIT?

The FDA product code for ZEFON ADULT ANESTHESIA 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 Zefon Medical Products 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.

K940220REBREATHER BAGSK934462ADULT ANESTHESIA BREATHING CIRCUIT KITSK930957ZEFON GAS SAMPLING LINES

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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