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FDA 510(k)

SYNTERMED LIVE

K-Number: K070089 · 2007-03-02

ApplicantSyntermed, Inc.
Decision Date2007-03-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNTERMED LIVE is the device name listed in this FDA 510(k) record. The listed applicant is Syntermed, Inc.. It received FDA 510(k) clearance on 2007-03-02 under 510(k) number K070089. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTERMED LIVE?

SYNTERMED LIVE is a medical device that received FDA 510(k) clearance on 2007-03-02. The listed applicant is Syntermed, Inc.. The 510(k) number is K070089.

When did SYNTERMED LIVE receive FDA 510(k) clearance?

SYNTERMED LIVE received FDA 510(k) clearance on 2007-03-02, under 510(k) number K070089.

Who is the listed applicant for SYNTERMED LIVE?

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

What is the FDA product code for SYNTERMED LIVE?

The FDA product code for SYNTERMED LIVE is LLZ.

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Other records listing Syntermed, Inc. as applicant

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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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