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FDA 510(k)

MODELS LYNX AND PANTHER MOTORIZED SCOOTERS

K-Number: K992052 · 1999-08-12

ApplicantInvacare Corp.
Decision Date1999-08-12
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODELS LYNX AND PANTHER MOTORIZED SCOOTERS is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1999-08-12 under 510(k) number K992052. 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 MODELS LYNX AND PANTHER MOTORIZED SCOOTERS?

MODELS LYNX AND PANTHER MOTORIZED SCOOTERS is a medical device that received FDA 510(k) clearance on 1999-08-12. The listed applicant is Invacare Corp.. The 510(k) number is K992052.

When did MODELS LYNX AND PANTHER MOTORIZED SCOOTERS receive FDA 510(k) clearance?

MODELS LYNX AND PANTHER MOTORIZED SCOOTERS received FDA 510(k) clearance on 1999-08-12, under 510(k) number K992052.

Who is the listed applicant for MODELS LYNX AND PANTHER MOTORIZED SCOOTERS?

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

What is the FDA product code for MODELS LYNX AND PANTHER MOTORIZED SCOOTERS?

The FDA product code for MODELS LYNX AND PANTHER MOTORIZED SCOOTERS is INI.

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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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