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FDA 510(k)

ADULT ANESTHESIA BREATHING CIRCUIT KITS

K-Number: K934462 · 1994-03-01

ApplicantZefon Medical Products
Decision Date1994-03-01
Product CodeCAI
Advisory CommitteeAN
DecisionUnknown

Device Summary

ADULT ANESTHESIA BREATHING CIRCUIT KITS 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 1994-03-01 under 510(k) number K934462. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ADULT ANESTHESIA BREATHING CIRCUIT KITS?

ADULT ANESTHESIA BREATHING CIRCUIT KITS is a medical device that received FDA 510(k) clearance on 1994-03-01. The listed applicant is Zefon Medical Products. The 510(k) number is K934462.

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

ADULT ANESTHESIA BREATHING CIRCUIT KITS received FDA 510(k) clearance on 1994-03-01, under 510(k) number K934462.

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

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 ADULT ANESTHESIA BREATHING CIRCUIT KITS?

The FDA product code for ADULT ANESTHESIA BREATHING CIRCUIT KITS 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 BAGSK930957ZEFON GAS SAMPLING LINESK924889ZEFON ADULT ANESTHESIA BREATHING CIRCUIT

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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