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FDA 510(k)

RK VACUUM FIXATION RING SYSTEM

K-Number: K863775 · 1986-10-20

ApplicantAmeritek, Inc.
Decision Date1986-10-20
Product CodeHNH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RK VACUUM FIXATION RING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ameritek, Inc.. It received FDA 510(k) clearance on 1986-10-20 under 510(k) number K863775. The device is classified under product code HNH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RK VACUUM FIXATION RING SYSTEM?

RK VACUUM FIXATION RING SYSTEM is a medical device that received FDA 510(k) clearance on 1986-10-20. The listed applicant is Ameritek, Inc.. The 510(k) number is K863775.

When did RK VACUUM FIXATION RING SYSTEM receive FDA 510(k) clearance?

RK VACUUM FIXATION RING SYSTEM received FDA 510(k) clearance on 1986-10-20, under 510(k) number K863775.

Who is the listed applicant for RK VACUUM FIXATION RING SYSTEM?

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

What is the FDA product code for RK VACUUM FIXATION RING SYSTEM?

The FDA product code for RK VACUUM FIXATION RING SYSTEM is HNH.

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Related Devices (Code: HNH)

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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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