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FDA 510(k)

COREFORM MOLDS

K-Number: K801530 · 1980-07-28

ApplicantSybron Corp.
Decision Date1980-07-28
Product CodeDZN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COREFORM MOLDS is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1980-07-28 under 510(k) number K801530. The device is classified under product code DZN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COREFORM MOLDS?

COREFORM MOLDS is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Sybron Corp.. The 510(k) number is K801530.

When did COREFORM MOLDS receive FDA 510(k) clearance?

COREFORM MOLDS received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801530.

Who is the listed applicant for COREFORM MOLDS?

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 COREFORM MOLDS?

The FDA product code for COREFORM MOLDS is DZN.

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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: DZN)

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.

K111465COMPOTHIXOKerrhawe SAK071858DENTAL MATRIX BANDFly Cast Technologies, Inc.K901919CONTACT MOLAR BANDS AND CONTOUR STRIPSIvoclar North America, Inc.K861581CENTRIX PCR MOLAR MATRIX FORMS (BANDS)Centrix, Inc.K844324TIGER BANDWorld Wide Outdoor MarketingK840984INTERDENTAL WEDGESHealthco, Inc.

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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