FDA 510(k)

REPLICA BONDING AGENT

K-Number: K771881 · 1977-11-09

Decision Date1977-11-09

Product Code

DecisionSubstantially Equivalent

Device Summary

REPLICA BONDING AGENT is the device name listed in this FDA 510(k) record. The listed applicant is Hoyt Laboratories. It received FDA 510(k) clearance on 1977-11-09 under 510(k) number K771881. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLICA BONDING AGENT?

REPLICA BONDING AGENT is a medical device that received FDA 510(k) clearance on 1977-11-09. The listed applicant is Hoyt Laboratories. The 510(k) number is K771881.

When did REPLICA BONDING AGENT receive FDA 510(k) clearance?

REPLICA BONDING AGENT received FDA 510(k) clearance on 1977-11-09, under 510(k) number K771881.

Who is the listed applicant for REPLICA BONDING AGENT?

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

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Other records listing Hoyt Laboratories as applicant

K820738LUSTRALLOY K811154HOYT ECONO-TRAY K810830HOYT COTTON ROLLS K780834PREVI DENT PROPHYLAXIS MINT NDC K771883REPLICA ACID-ETCH K771882REPLICA DENTAL COMPOSITE-RADIOPAQUE

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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.