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FDA 510(k)

CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE)

K-Number: K890822 · 1989-05-05

ApplicantVentlab Corp.
Decision Date1989-05-05
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE) is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 1989-05-05 under 510(k) number K890822. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE)?

CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE) is a medical device that received FDA 510(k) clearance on 1989-05-05. The listed applicant is Ventlab Corp.. The 510(k) number is K890822.

When did CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE) receive FDA 510(k) clearance?

CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE) received FDA 510(k) clearance on 1989-05-05, under 510(k) number K890822.

Who is the listed applicant for CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE)?

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

What is the FDA product code for CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE)?

The FDA product code for CIRCUIT BREATHING (W CONNECTOR, ADAPTER Y PIECE) is BZO.

Related Clinical Trials

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Other records listing Ventlab Corp. 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.

K120118VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETERK102674CUFF SENTRYK093617VENTLAB 6000 SERIES HUMIDIFIERK093525ACE/STATCHECK II CO2 INDICATOR, ACE/STATCHECK II CO2 INDICATOR ARM ASSEMBY ADULT STATCHECK RESUSCITATOR WITH ACE/STATCHEK090840VENTLAB 5000 SERIES NEBULIZER ASSEMBLY, CUP, CUP W/ MASK, CUP W/ FITSALL CONN.K082204SERIES SY DISPOSABLE ELECTROSURGICAL PAD

View all 22 devices →

Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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