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FDA 510(k)

QUANTUM BLAST

K-Number: K011993 · 2001-07-13

ApplicantPride Mobility Products Corp.
Decision Date2001-07-13
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUANTUM BLAST 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 2001-07-13 under 510(k) number K011993. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTUM BLAST?

QUANTUM BLAST is a medical device that received FDA 510(k) clearance on 2001-07-13. The listed applicant is Pride Mobility Products Corp.. The 510(k) number is K011993.

When did QUANTUM BLAST receive FDA 510(k) clearance?

QUANTUM BLAST received FDA 510(k) clearance on 2001-07-13, under 510(k) number K011993.

Who is the listed applicant for QUANTUM BLAST?

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 QUANTUM BLAST?

The FDA product code for QUANTUM BLAST is ITI.

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Related Devices (Code: ITI)

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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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