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FDA 510(k)

INTERTECH LARGE VOLUME WATER TRAP (LVW)

K-Number: K882739 · 1988-08-09

ApplicantIntertech Resources, Inc.
Decision Date1988-08-09
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTERTECH LARGE VOLUME WATER TRAP (LVW) is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1988-08-09 under 510(k) number K882739. 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 INTERTECH LARGE VOLUME WATER TRAP (LVW)?

INTERTECH LARGE VOLUME WATER TRAP (LVW) is a medical device that received FDA 510(k) clearance on 1988-08-09. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K882739.

When did INTERTECH LARGE VOLUME WATER TRAP (LVW) receive FDA 510(k) clearance?

INTERTECH LARGE VOLUME WATER TRAP (LVW) received FDA 510(k) clearance on 1988-08-09, under 510(k) number K882739.

Who is the listed applicant for INTERTECH LARGE VOLUME WATER TRAP (LVW)?

The FDA 510(k) record lists Intertech Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERTECH LARGE VOLUME WATER TRAP (LVW)?

The FDA product code for INTERTECH LARGE VOLUME WATER TRAP (LVW) is BYH.

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Other records listing Intertech Resources, Inc. 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.

K9613181ST RESPONSE DISPOSABLE MANOMETERK955008HEAT & MOISTURE EXCHANGERK953580HEAT MOISTURE EXCHANGERK952223XENON GAS BREATHING CIRCUITK952062PFT FILTERK952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC

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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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