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FDA 510(k)

POST TRAY

K-Number: K863836 · 1986-10-14

ApplicantMarket Masters, Inc.
Decision Date1986-10-14
Product CodeEHY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POST TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Market Masters, Inc.. It received FDA 510(k) clearance on 1986-10-14 under 510(k) number K863836. 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 POST TRAY?

POST TRAY is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Market Masters, Inc.. The 510(k) number is K863836.

When did POST TRAY receive FDA 510(k) clearance?

POST TRAY received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863836.

Who is the listed applicant for POST TRAY?

The FDA 510(k) record lists Market Masters, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POST TRAY?

The FDA product code for POST TRAY is EHY.

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.

K942668O-TRAY IMPRESSION TRAYSDentauraum, Inc.K896470EOS IMPRESSION TRAYSIvoclar North America, Inc.K884316OCCLUSAL HARMONY IMPRESSION TRAYAdvantage Dental Co.K850776PREFORMED DENTAL IMPRESSION TRAYSL.A.K. Ent., Inc.K842273CROWN INDEX TRAYDi-Equi Dental ProductsK842274F-G-P TRAYDi-Equi Dental Products

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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