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FDA 510(k)

H-H BURR HOLE CATHETER SUPPORT

K-Number: K820311 · 1982-02-24

ApplicantHolter-Hausner Intl.
Decision Date1982-02-24
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

H-H BURR HOLE CATHETER SUPPORT 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 1982-02-24 under 510(k) number K820311. 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 BURR HOLE CATHETER SUPPORT?

H-H BURR HOLE CATHETER SUPPORT is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Holter-Hausner Intl.. The 510(k) number is K820311.

When did H-H BURR HOLE CATHETER SUPPORT receive FDA 510(k) clearance?

H-H BURR HOLE CATHETER SUPPORT received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820311.

Who is the listed applicant for H-H BURR HOLE CATHETER SUPPORT?

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 BURR HOLE CATHETER SUPPORT?

The FDA product code for H-H BURR HOLE CATHETER SUPPORT is JXG.

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Related Devices (Code: JXG)

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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