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FDA 510(k)

4-IN-1 DISP. CROWN & BRIDGE TRAY

K-Number: K780211 · 1978-02-16

ApplicantKerr Corporation (Danbury)
Decision Date1978-02-16
Product CodeEHY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

4-IN-1 DISP. CROWN & BRIDGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation (Danbury). It received FDA 510(k) clearance on 1978-02-16 under 510(k) number K780211. The device is classified under product code EHY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 4-IN-1 DISP. CROWN & BRIDGE TRAY?

4-IN-1 DISP. CROWN & BRIDGE TRAY is a medical device that received FDA 510(k) clearance on 1978-02-16. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K780211.

When did 4-IN-1 DISP. CROWN & BRIDGE TRAY receive FDA 510(k) clearance?

4-IN-1 DISP. CROWN & BRIDGE TRAY received FDA 510(k) clearance on 1978-02-16, under 510(k) number K780211.

Who is the listed applicant for 4-IN-1 DISP. CROWN & BRIDGE TRAY?

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

What is the FDA product code for 4-IN-1 DISP. CROWN & BRIDGE TRAY?

The FDA product code for 4-IN-1 DISP. CROWN & BRIDGE TRAY is EHY.

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Related Devices (Code: EHY)

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.

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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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