FDA · official record K900809Substantially Equivalent

LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS

Name: LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS — FDA K900809
Creator: Lee Pharmaceuticals
Keywords: LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS, LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS, K900809, DYW, FDA

United StatesDYWLee Pharmaceuticals

Verified

Official record identity

FDA application number: K900809
Decision date: June 28, 1990
Published decision: Substantially Equivalent

Classification

Product code: DYW

Published parties

Applicant: Lee Pharmaceuticals

Additional source fields

Decision code: SESE
Published decision: Substantially Equivalent
Submission type: Traditional
Received date: 1990-02-21
Review panel: Dental
Current product-code class (harmonized): 2
Current product-code regulation (harmonized): 872.5470

About this record

This record preserves an application published in the FDA 510(k) bulk export, including the DEN entries FDA includes in that export. Historical decisions do not establish current marketing status. Product-code harmonization is separate from the original application; joined establishment identifiers are not assigned to the applicant. The complete official export is checked daily and raw evidence is retained.