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FDA 510(k)

SURE GRIP, HAND CONTROLS MODEL SG-1

K-Number: K910072 · 1991-01-23

Decision Date1991-01-23
Product CodeIPQ
DecisionSubstantially Equivalent

Device Summary

SURE GRIP, HAND CONTROLS MODEL SG-1 is the device name listed in this FDA 510(k) record. The listed applicant is Howell Ventures , Ltd.. It received FDA 510(k) clearance on 1991-01-23 under 510(k) number K910072. The device is classified under product code IPQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURE GRIP, HAND CONTROLS MODEL SG-1?

SURE GRIP, HAND CONTROLS MODEL SG-1 is a medical device that received FDA 510(k) clearance on 1991-01-23. The listed applicant is Howell Ventures , Ltd.. The 510(k) number is K910072.

When did SURE GRIP, HAND CONTROLS MODEL SG-1 receive FDA 510(k) clearance?

SURE GRIP, HAND CONTROLS MODEL SG-1 received FDA 510(k) clearance on 1991-01-23, under 510(k) number K910072.

Who is the listed applicant for SURE GRIP, HAND CONTROLS MODEL SG-1?

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

What is the FDA product code for SURE GRIP, HAND CONTROLS MODEL SG-1?

The FDA product code for SURE GRIP, HAND CONTROLS MODEL SG-1 is IPQ.

Related Clinical Trials

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.

Related Devices (Code: IPQ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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