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FDA 510(k)

MYERSONS SPEC. CROWN & BRIDGE RESIN

K-Number: K771602 · 1977-08-30

ApplicantHowmedica Corp.
Decision Date1977-08-30
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MYERSONS SPEC. CROWN & BRIDGE RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1977-08-30 under 510(k) number K771602. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYERSONS SPEC. CROWN & BRIDGE RESIN?

MYERSONS SPEC. CROWN & BRIDGE RESIN is a medical device that received FDA 510(k) clearance on 1977-08-30. The listed applicant is Howmedica Corp.. The 510(k) number is K771602.

When did MYERSONS SPEC. CROWN & BRIDGE RESIN receive FDA 510(k) clearance?

MYERSONS SPEC. CROWN & BRIDGE RESIN received FDA 510(k) clearance on 1977-08-30, under 510(k) number K771602.

Who is the listed applicant for MYERSONS SPEC. CROWN & BRIDGE RESIN?

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

What is the FDA product code for MYERSONS SPEC. CROWN & BRIDGE RESIN?

The FDA product code for MYERSONS SPEC. CROWN & BRIDGE RESIN is EBG.

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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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