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FDA 510(k)

BOOSTER LITE 3 MOTORIZED SCOOTER

K-Number: K955274 · 1996-11-04

ApplicantOptimed Technologies, Inc.
Decision Date1996-11-04
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BOOSTER LITE 3 MOTORIZED SCOOTER is the device name listed in this FDA 510(k) record. The listed applicant is Optimed Technologies, Inc.. It received FDA 510(k) clearance on 1996-11-04 under 510(k) number K955274. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOOSTER LITE 3 MOTORIZED SCOOTER?

BOOSTER LITE 3 MOTORIZED SCOOTER is a medical device that received FDA 510(k) clearance on 1996-11-04. The listed applicant is Optimed Technologies, Inc.. The 510(k) number is K955274.

When did BOOSTER LITE 3 MOTORIZED SCOOTER receive FDA 510(k) clearance?

BOOSTER LITE 3 MOTORIZED SCOOTER received FDA 510(k) clearance on 1996-11-04, under 510(k) number K955274.

Who is the listed applicant for BOOSTER LITE 3 MOTORIZED SCOOTER?

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

What is the FDA product code for BOOSTER LITE 3 MOTORIZED SCOOTER?

The FDA product code for BOOSTER LITE 3 MOTORIZED SCOOTER is INI.

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Other records listing Optimed Technologies, Inc. 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.

K972520OPTIVIEWK955276BOOSTER LITE 4 MOTORIZED SCOOTERK955275BOOSTER TROPHY 5 MOTORIZED SCOOTERK943598FLEXIBLE FIBER OPTIC LAPAROSCOPESK926597LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)K921942HYSTEROSCOPE (AND ACCESSORIES)

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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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