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FDA 510(k)

CONVENTIONAL PLASTIC DENTAL TRAYS

K-Number: K841491 · 1984-07-13

Decision Date1984-07-13
Product CodeEHY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CONVENTIONAL PLASTIC DENTAL TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Buffalo Dental Mfg. Co., Inc.. It received FDA 510(k) clearance on 1984-07-13 under 510(k) number K841491. 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 CONVENTIONAL PLASTIC DENTAL TRAYS?

CONVENTIONAL PLASTIC DENTAL TRAYS is a medical device that received FDA 510(k) clearance on 1984-07-13. The listed applicant is Buffalo Dental Mfg. Co., Inc.. The 510(k) number is K841491.

When did CONVENTIONAL PLASTIC DENTAL TRAYS receive FDA 510(k) clearance?

CONVENTIONAL PLASTIC DENTAL TRAYS received FDA 510(k) clearance on 1984-07-13, under 510(k) number K841491.

Who is the listed applicant for CONVENTIONAL PLASTIC DENTAL TRAYS?

The FDA 510(k) record lists Buffalo Dental Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVENTIONAL PLASTIC DENTAL TRAYS?

The FDA product code for CONVENTIONAL PLASTIC DENTAL TRAYS is EHY.

Related Clinical Trials

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.

Other records listing Buffalo Dental Mfg. Co., Inc. 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.

View all 11 devices →

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.

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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