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FDA 510(k)

INFINET

K-Number: K961689 · 1996-07-31

ApplicantInfimed, Inc.
Decision Date1996-07-31
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INFINET is the device name listed in this FDA 510(k) record. The listed applicant is Infimed, Inc.. It received FDA 510(k) clearance on 1996-07-31 under 510(k) number K961689. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFINET?

INFINET is a medical device that received FDA 510(k) clearance on 1996-07-31. The listed applicant is Infimed, Inc.. The 510(k) number is K961689.

When did INFINET receive FDA 510(k) clearance?

INFINET received FDA 510(k) clearance on 1996-07-31, under 510(k) number K961689.

Who is the listed applicant for INFINET?

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 INFINET?

The FDA product code for INFINET is LMD.

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Other records listing Infimed, Inc. as applicant

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Related Devices (Code: LMD)

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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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