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FDA 510(k)

QL MULTIPULSE 2048

K-Number: K933299 · 1993-11-03

ApplicantInfimed, Inc.
Decision Date1993-11-03
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QL MULTIPULSE 2048 is the device name listed in this FDA 510(k) record. The listed applicant is Infimed, Inc.. It received FDA 510(k) clearance on 1993-11-03 under 510(k) number K933299. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QL MULTIPULSE 2048?

QL MULTIPULSE 2048 is a medical device that received FDA 510(k) clearance on 1993-11-03. The listed applicant is Infimed, Inc.. The 510(k) number is K933299.

When did QL MULTIPULSE 2048 receive FDA 510(k) clearance?

QL MULTIPULSE 2048 received FDA 510(k) clearance on 1993-11-03, under 510(k) number K933299.

Who is the listed applicant for QL MULTIPULSE 2048?

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

What is the FDA product code for QL MULTIPULSE 2048?

The FDA product code for QL MULTIPULSE 2048 is JAA.

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Related Devices (Code: JAA)

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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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