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FDA 510(k)

BOOST, MICE, GAMESYS.

K-Number: K924416 · 1993-06-15

ApplicantPenny and Giles Biometrics , Ltd.
Decision Date1993-06-15
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BOOST, MICE, GAMESYS. is the device name listed in this FDA 510(k) record. The listed applicant is Penny and Giles Biometrics , Ltd.. It received FDA 510(k) clearance on 1993-06-15 under 510(k) number K924416. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOOST, MICE, GAMESYS.?

BOOST, MICE, GAMESYS. is a medical device that received FDA 510(k) clearance on 1993-06-15. The listed applicant is Penny and Giles Biometrics , Ltd.. The 510(k) number is K924416.

When did BOOST, MICE, GAMESYS. receive FDA 510(k) clearance?

BOOST, MICE, GAMESYS. received FDA 510(k) clearance on 1993-06-15, under 510(k) number K924416.

Who is the listed applicant for BOOST, MICE, GAMESYS.?

The FDA 510(k) record lists Penny and Giles Biometrics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOOST, MICE, GAMESYS.?

The FDA product code for BOOST, MICE, GAMESYS. is KQX.

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.

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Other records listing Penny and Giles Biometrics , Ltd. as applicant

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.

K962855ULE-2, MULE-2, HAND ACCESSORY KITK934238MULE

Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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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