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FDA 510(k)

MATERIAL ADDITION LEXAN & K-RESIN

K-Number: K833554 · 1984-03-12

ApplicantProcedure Products, Inc.
Decision Date1984-03-12
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MATERIAL ADDITION LEXAN & K-RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Procedure Products, Inc.. It received FDA 510(k) clearance on 1984-03-12 under 510(k) number K833554. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATERIAL ADDITION LEXAN & K-RESIN?

MATERIAL ADDITION LEXAN & K-RESIN is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is Procedure Products, Inc.. The 510(k) number is K833554.

When did MATERIAL ADDITION LEXAN & K-RESIN receive FDA 510(k) clearance?

MATERIAL ADDITION LEXAN & K-RESIN received FDA 510(k) clearance on 1984-03-12, under 510(k) number K833554.

Who is the listed applicant for MATERIAL ADDITION LEXAN & K-RESIN?

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

What is the FDA product code for MATERIAL ADDITION LEXAN & K-RESIN?

The FDA product code for MATERIAL ADDITION LEXAN & K-RESIN is DQO.

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Related Devices (Code: DQO)

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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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