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FDA 510(k)

JET VENTILATION ADAPTOR

K-Number: K842456 · 1984-07-06

ApplicantPortex, Inc.
Decision Date1984-07-06
Product Code
DecisionSubstantially Equivalent

Device Summary

JET VENTILATION ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Portex, Inc.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K842456. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JET VENTILATION ADAPTOR?

JET VENTILATION ADAPTOR is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Portex, Inc.. The 510(k) number is K842456.

When did JET VENTILATION ADAPTOR receive FDA 510(k) clearance?

JET VENTILATION ADAPTOR received FDA 510(k) clearance on 1984-07-06, under 510(k) number K842456.

Who is the listed applicant for JET VENTILATION ADAPTOR?

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

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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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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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