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FDA 510(k)

TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE

K-Number: K896439 · 1990-01-09

ApplicantVentlab Corp.
Decision Date1990-01-09
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 1990-01-09 under 510(k) number K896439. 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 TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE?

TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE is a medical device that received FDA 510(k) clearance on 1990-01-09. The listed applicant is Ventlab Corp.. The 510(k) number is K896439.

When did TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE receive FDA 510(k) clearance?

TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE received FDA 510(k) clearance on 1990-01-09, under 510(k) number K896439.

Who is the listed applicant for TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE?

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 TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE?

The FDA product code for TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE is BZO.

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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

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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.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952011PRIMA BREATHING BAGSPrima, 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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