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FDA 510(k)

CAPMIX

K-Number: K771901 · 1977-10-20

ApplicantEspe Dental Products
Decision Date1977-10-20
Product CodeEFD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAPMIX is the device name listed in this FDA 510(k) record. The listed applicant is Espe Dental Products. It received FDA 510(k) clearance on 1977-10-20 under 510(k) number K771901. The device is classified under product code EFD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPMIX?

CAPMIX is a medical device that received FDA 510(k) clearance on 1977-10-20. The listed applicant is Espe Dental Products. The 510(k) number is K771901.

When did CAPMIX receive FDA 510(k) clearance?

CAPMIX received FDA 510(k) clearance on 1977-10-20, under 510(k) number K771901.

Who is the listed applicant for CAPMIX?

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

What is the FDA product code for CAPMIX?

The FDA product code for CAPMIX is EFD.

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Other records listing Espe Dental Products 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.

K810950VISIO-SEALK802819KETAC-CEM IN REF. TO K802048K802049NIMETIC-DISPERSK800031PERMADYNE POLYETHER RUBBER IMPRESSIONK771889UNIOLITEK771120IMPREFLEX ALGINATE IMPRESSION MATERIAL

View all 8 devices →

Related Devices (Code: EFD)

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.

K991913PENTAMIX 2Espe Dental AGK923974SILIMAT PLUSIvoclar North America, Inc.K922203IPT CAPSULE MIXERIpt Technologies, Inc.K915847AUTOMIX DENTAL AMALGAMATORKerr Corporation (Danbury)K914341MIXOMAT AMALGAMATORDegussa AGK914340DUOMAT 3 AMALGAMATORDegussa AG

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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