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FDA 510(k)

ANESTHESIA BREATHING CIRCUIT

K-Number: K900594 · 1990-03-15

ApplicantInhalation Plastics
Decision Date1990-03-15
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Inhalation Plastics. It received FDA 510(k) clearance on 1990-03-15 under 510(k) number K900594. 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 ANESTHESIA BREATHING CIRCUIT?

ANESTHESIA BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1990-03-15. The listed applicant is Inhalation Plastics. The 510(k) number is K900594.

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

ANESTHESIA BREATHING CIRCUIT received FDA 510(k) clearance on 1990-03-15, under 510(k) number K900594.

Who is the listed applicant for ANESTHESIA BREATHING CIRCUIT?

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

What is the FDA product code for ANESTHESIA BREATHING CIRCUIT?

The FDA product code for ANESTHESIA BREATHING CIRCUIT is CAI.

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Other records listing Inhalation Plastics 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.

K945565SPIRO-FLEXK914686THERMO-FLOW SETK901315AEROMIST II NEBULIZERK900990FILT-R-ALL BACTERIAL/VIRAL FILTERK896832FILT-R-ALL BACTERIAL FILTERK874659STERILIZATION OF DEVICES BY RADIATION

View all 7 devices →

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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