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FDA 510(k)

JOSTRA VENT CATHETERS, MODELS LV & HKV

K-Number: K022022 · 2002-09-11

ApplicantJostra AG
Decision Date2002-09-11
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JOSTRA VENT CATHETERS, MODELS LV & HKV is the device name listed in this FDA 510(k) record. The listed applicant is Jostra AG. It received FDA 510(k) clearance on 2002-09-11 under 510(k) number K022022. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOSTRA VENT CATHETERS, MODELS LV & HKV?

JOSTRA VENT CATHETERS, MODELS LV & HKV is a medical device that received FDA 510(k) clearance on 2002-09-11. The listed applicant is Jostra AG. The 510(k) number is K022022.

When did JOSTRA VENT CATHETERS, MODELS LV & HKV receive FDA 510(k) clearance?

JOSTRA VENT CATHETERS, MODELS LV & HKV received FDA 510(k) clearance on 2002-09-11, under 510(k) number K022022.

Who is the listed applicant for JOSTRA VENT CATHETERS, MODELS LV & HKV?

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

What is the FDA product code for JOSTRA VENT CATHETERS, MODELS LV & HKV?

The FDA product code for JOSTRA VENT CATHETERS, MODELS LV & HKV is DWF.

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Other records listing Jostra AG as applicant

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Related Devices (Code: DWF)

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.

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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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