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FDA 510(k)

LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS

K-Number: K900809 · 1990-06-28

ApplicantLee Pharmaceuticals
Decision Date1990-06-28
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1990-06-28 under 510(k) number K900809. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS?

LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS is a medical device that received FDA 510(k) clearance on 1990-06-28. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K900809.

When did LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS receive FDA 510(k) clearance?

LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS received FDA 510(k) clearance on 1990-06-28, under 510(k) number K900809.

Who is the listed applicant for LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS?

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

What is the FDA product code for LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS?

The FDA product code for LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS is DYW.

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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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