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FDA 510(k)

THERMOVENT 600, 1200, T, 02

K-Number: K874597 · 1988-01-19

ApplicantPortex, Inc.
Decision Date1988-01-19
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THERMOVENT 600, 1200, T, 02 is the device name listed in this FDA 510(k) record. The listed applicant is Portex, Inc.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K874597. The device is classified under product code BYD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMOVENT 600, 1200, T, 02?

THERMOVENT 600, 1200, T, 02 is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Portex, Inc.. The 510(k) number is K874597.

When did THERMOVENT 600, 1200, T, 02 receive FDA 510(k) clearance?

THERMOVENT 600, 1200, T, 02 received FDA 510(k) clearance on 1988-01-19, under 510(k) number K874597.

Who is the listed applicant for THERMOVENT 600, 1200, T, 02?

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

What is the FDA product code for THERMOVENT 600, 1200, T, 02?

The FDA product code for THERMOVENT 600, 1200, T, 02 is BYD.

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Other records listing Portex, 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.

K033080PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETERK031057PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KITK0237931ST RESPONSE INTERMEDIATE MANUAL RESUSCITATORK0141151ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XXK014073HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICEK873992LARYNGECTOMY TUBE

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Related Devices (Code: BYD)

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.

K955008HEAT & MOISTURE EXCHANGERIntertech Resources, Inc.K954194DISPOSABLE HME/FILTEREngstrom MedicalK953580HEAT MOISTURE EXCHANGERIntertech Resources, Inc.K953507TYPE 1 & 2 (HUMIDAIR I & II)Icor ABK953544HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHTGibeck, Inc.K953620WARM N WET HMEF W/LUER ADAPTERHospitak, 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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