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FDA 510(k)

H-H IN-LINE VALVED CATHETER 2 TYPES

K-Number: K830894 · 1983-04-08

ApplicantHolter-Hausner Intl.
Decision Date1983-04-08
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

H-H IN-LINE VALVED CATHETER 2 TYPES is the device name listed in this FDA 510(k) record. The listed applicant is Holter-Hausner Intl.. It received FDA 510(k) clearance on 1983-04-08 under 510(k) number K830894. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H-H IN-LINE VALVED CATHETER 2 TYPES?

H-H IN-LINE VALVED CATHETER 2 TYPES is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Holter-Hausner Intl.. The 510(k) number is K830894.

When did H-H IN-LINE VALVED CATHETER 2 TYPES receive FDA 510(k) clearance?

H-H IN-LINE VALVED CATHETER 2 TYPES received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830894.

Who is the listed applicant for H-H IN-LINE VALVED CATHETER 2 TYPES?

The FDA 510(k) record lists Holter-Hausner Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for H-H IN-LINE VALVED CATHETER 2 TYPES?

The FDA product code for H-H IN-LINE VALVED CATHETER 2 TYPES is JXG.

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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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