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FDA 510(k)

BLD-18000 SERIES HEATED BREATHING CIRCUIT

K-Number: K925543 · 1993-04-30

ApplicantBird Life Design
Decision Date1993-04-30
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BLD-18000 SERIES HEATED BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Bird Life Design. It received FDA 510(k) clearance on 1993-04-30 under 510(k) number K925543. 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 BLD-18000 SERIES HEATED BREATHING CIRCUIT?

BLD-18000 SERIES HEATED BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1993-04-30. The listed applicant is Bird Life Design. The 510(k) number is K925543.

When did BLD-18000 SERIES HEATED BREATHING CIRCUIT receive FDA 510(k) clearance?

BLD-18000 SERIES HEATED BREATHING CIRCUIT received FDA 510(k) clearance on 1993-04-30, under 510(k) number K925543.

Who is the listed applicant for BLD-18000 SERIES HEATED BREATHING CIRCUIT?

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

What is the FDA product code for BLD-18000 SERIES HEATED BREATHING CIRCUIT?

The FDA product code for BLD-18000 SERIES HEATED BREATHING CIRCUIT is CAI.

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Other records listing Bird Life Design 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.

K931487BLD HEATED BREATHING CIRCUIT W/EXHALATION VALVEK934190HME W/O FILTER HYGROFLEX, HYGROFLEX-T, MODIFICATIONK934189BARRIERFLEX-I, AND BARRIERFLES-IIK934540BARRIERFLEX-PF PULMONARY FUNCTION TESTING FILTERK933641BLD NEONATAL HEATED WIRE BREATHING CIRCUIT- 30 VOLT COMPATIBLEK930252BABYSET AND PAC (PULMONARY ASSIST CIRCUIT)

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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