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FDA 510(k)

VENT-TRAP CAT# WR1000

K-Number: K900591 · 1990-03-09

ApplicantVentlab Corp.
Decision Date1990-03-09
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENT-TRAP CAT# WR1000 is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 1990-03-09 under 510(k) number K900591. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENT-TRAP CAT# WR1000?

VENT-TRAP CAT# WR1000 is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Ventlab Corp.. The 510(k) number is K900591.

When did VENT-TRAP CAT# WR1000 receive FDA 510(k) clearance?

VENT-TRAP CAT# WR1000 received FDA 510(k) clearance on 1990-03-09, under 510(k) number K900591.

Who is the listed applicant for VENT-TRAP CAT# WR1000?

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 VENT-TRAP CAT# WR1000?

The FDA product code for VENT-TRAP CAT# WR1000 is BYH.

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: BYH)

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.

K946057AQUALARM MOISTURE SENSOR MODEL P85000Pegasus Research Corp.K932722CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEMCarie Med-Tech Services, Inc.K921624DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITSIntertech Resources, Inc.K900047THAYER SUCTION EVACUATION CONDENSATE COLLECTIONThayer Medical Corp.K897057THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEMThayer Medical Corp.K895479THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEMThayer Medical Corp.

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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