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FDA 510(k)

SURGITA/MIZHO MICRONEUROSURGERY HEAD FR

K-Number: K821772 · 1982-09-28

ApplicantDowns Surgical , Ltd.
Decision Date1982-09-28
Product CodeHBL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SURGITA/MIZHO MICRONEUROSURGERY HEAD FR is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1982-09-28 under 510(k) number K821772. The device is classified under product code HBL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGITA/MIZHO MICRONEUROSURGERY HEAD FR?

SURGITA/MIZHO MICRONEUROSURGERY HEAD FR is a medical device that received FDA 510(k) clearance on 1982-09-28. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K821772.

When did SURGITA/MIZHO MICRONEUROSURGERY HEAD FR receive FDA 510(k) clearance?

SURGITA/MIZHO MICRONEUROSURGERY HEAD FR received FDA 510(k) clearance on 1982-09-28, under 510(k) number K821772.

Who is the listed applicant for SURGITA/MIZHO MICRONEUROSURGERY HEAD FR?

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

What is the FDA product code for SURGITA/MIZHO MICRONEUROSURGERY HEAD FR?

The FDA product code for SURGITA/MIZHO MICRONEUROSURGERY HEAD FR is HBL.

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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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