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FDA 510(k)

SYBRON/KERR CONTOUR

K-Number: K820181 · 1982-02-24

ApplicantSybron Corp.
Decision Date1982-02-24
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYBRON/KERR CONTOUR is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1982-02-24 under 510(k) number K820181. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYBRON/KERR CONTOUR?

SYBRON/KERR CONTOUR is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Sybron Corp.. The 510(k) number is K820181.

When did SYBRON/KERR CONTOUR receive FDA 510(k) clearance?

SYBRON/KERR CONTOUR received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820181.

Who is the listed applicant for SYBRON/KERR CONTOUR?

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

What is the FDA product code for SYBRON/KERR CONTOUR?

The FDA product code for SYBRON/KERR CONTOUR is EJJ.

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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

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Related Devices (Code: EJJ)

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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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