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FDA 510(k)

COMMAND BONDING RESIN/GLAZE/OPAQUER

K-Number: K822869 · 1982-10-13

ApplicantSybron Corp.
Decision Date1982-10-13
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMMAND BONDING RESIN/GLAZE/OPAQUER is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1982-10-13 under 510(k) number K822869. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMMAND BONDING RESIN/GLAZE/OPAQUER?

COMMAND BONDING RESIN/GLAZE/OPAQUER is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is Sybron Corp.. The 510(k) number is K822869.

When did COMMAND BONDING RESIN/GLAZE/OPAQUER receive FDA 510(k) clearance?

COMMAND BONDING RESIN/GLAZE/OPAQUER received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822869.

Who is the listed applicant for COMMAND BONDING RESIN/GLAZE/OPAQUER?

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 COMMAND BONDING RESIN/GLAZE/OPAQUER?

The FDA product code for COMMAND BONDING RESIN/GLAZE/OPAQUER is EBD.

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Other records listing Sybron Corp. as applicant

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Related Devices (Code: EBD)

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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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