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FDA 510(k)

K-FLEX

K-Number: K811519 · 1981-06-26

ApplicantSybron Corp.
Decision Date1981-06-26
Product Code
DecisionSubstantially Equivalent

Device Summary

K-FLEX is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1981-06-26 under 510(k) number K811519. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-FLEX?

K-FLEX is a medical device that received FDA 510(k) clearance on 1981-06-26. The listed applicant is Sybron Corp.. The 510(k) number is K811519.

When did K-FLEX receive FDA 510(k) clearance?

K-FLEX received FDA 510(k) clearance on 1981-06-26, under 510(k) number K811519.

Who is the listed applicant for K-FLEX?

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

Other records listing Sybron Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K862284SEALITEK854855PROOF ALGINATE IMPRESSION MATERIALK844092DIAGNOSTIC MICROSOPCE SLIDESK842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOK841910KERR SEALAPEX ROOT CANAL SEALERK841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM

View all 37 devices →

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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