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FDA 510(k)

H-H NERVE ROOT RETRACTOR

K-Number: K822048 · 1982-07-22

ApplicantHolter-Hausner Intl.
Decision Date1982-07-22
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

H-H NERVE ROOT RETRACTOR 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 1982-07-22 under 510(k) number K822048. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H-H NERVE ROOT RETRACTOR?

H-H NERVE ROOT RETRACTOR is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Holter-Hausner Intl.. The 510(k) number is K822048.

When did H-H NERVE ROOT RETRACTOR receive FDA 510(k) clearance?

H-H NERVE ROOT RETRACTOR received FDA 510(k) clearance on 1982-07-22, under 510(k) number K822048.

Who is the listed applicant for H-H NERVE ROOT RETRACTOR?

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 NERVE ROOT RETRACTOR?

The FDA product code for H-H NERVE ROOT RETRACTOR is HAO.

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Related Devices (Code: HAO)

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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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