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FDA 510(k)

DIAGNOSTIC MICROSOPCE SLIDES

K-Number: K844092 · 1984-10-25

ApplicantSybron Corp.
Decision Date1984-10-25
Product Code
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC MICROSOPCE SLIDES is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1984-10-25 under 510(k) number K844092. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGNOSTIC MICROSOPCE SLIDES?

DIAGNOSTIC MICROSOPCE SLIDES is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is Sybron Corp.. The 510(k) number is K844092.

When did DIAGNOSTIC MICROSOPCE SLIDES receive FDA 510(k) clearance?

DIAGNOSTIC MICROSOPCE SLIDES received FDA 510(k) clearance on 1984-10-25, under 510(k) number K844092.

Who is the listed applicant for DIAGNOSTIC MICROSOPCE SLIDES?

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

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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 MATERIALK842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOK841910KERR SEALAPEX ROOT CANAL SEALERK841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILMK840407KERR RESIN BONDED BRIDGE CEMENT

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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