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FDA 510(k)

THUMBSHELPER POWER RING

K-Number: K864870 · 1987-02-12

ApplicantLevolon Company, Inc.
Decision Date1987-02-12
Product CodeLQX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THUMBSHELPER POWER RING is the device name listed in this FDA 510(k) record. The listed applicant is Levolon Company, Inc.. It received FDA 510(k) clearance on 1987-02-12 under 510(k) number K864870. The device is classified under product code LQX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THUMBSHELPER POWER RING?

THUMBSHELPER POWER RING is a medical device that received FDA 510(k) clearance on 1987-02-12. The listed applicant is Levolon Company, Inc.. The 510(k) number is K864870.

When did THUMBSHELPER POWER RING receive FDA 510(k) clearance?

THUMBSHELPER POWER RING received FDA 510(k) clearance on 1987-02-12, under 510(k) number K864870.

Who is the listed applicant for THUMBSHELPER POWER RING?

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

What is the FDA product code for THUMBSHELPER POWER RING?

The FDA product code for THUMBSHELPER POWER RING is LQX.

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Related Devices (Code: LQX)

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.

K945537T-GUARDMed ET AL Development

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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