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FDA 510(k)

LASER 3 SPSC300

K-Number: K003058 · 2001-03-08

ApplicantPride Mobility Products Corp.
Decision Date2001-03-08
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LASER 3 SPSC300 is the device name listed in this FDA 510(k) record. The listed applicant is Pride Mobility Products Corp.. It received FDA 510(k) clearance on 2001-03-08 under 510(k) number K003058. 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 LASER 3 SPSC300?

LASER 3 SPSC300 is a medical device that received FDA 510(k) clearance on 2001-03-08. The listed applicant is Pride Mobility Products Corp.. The 510(k) number is K003058.

When did LASER 3 SPSC300 receive FDA 510(k) clearance?

LASER 3 SPSC300 received FDA 510(k) clearance on 2001-03-08, under 510(k) number K003058.

Who is the listed applicant for LASER 3 SPSC300?

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

What is the FDA product code for LASER 3 SPSC300?

The FDA product code for LASER 3 SPSC300 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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