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FDA 510(k)

STINGRAY DR, MODEL 1

K-Number: K992794 · 1999-11-09

ApplicantInfimed, Inc.
Decision Date1999-11-09
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STINGRAY DR, MODEL 1 is the device name listed in this FDA 510(k) record. The listed applicant is Infimed, Inc.. It received FDA 510(k) clearance on 1999-11-09 under 510(k) number K992794. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STINGRAY DR, MODEL 1?

STINGRAY DR, MODEL 1 is a medical device that received FDA 510(k) clearance on 1999-11-09. The listed applicant is Infimed, Inc.. The 510(k) number is K992794.

When did STINGRAY DR, MODEL 1 receive FDA 510(k) clearance?

STINGRAY DR, MODEL 1 received FDA 510(k) clearance on 1999-11-09, under 510(k) number K992794.

Who is the listed applicant for STINGRAY DR, MODEL 1?

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 STINGRAY DR, MODEL 1?

The FDA product code for STINGRAY DR, MODEL 1 is MQB.

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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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