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FDA 510(k)

READI-LOAD SYSTEM, MODEL PSS 1820RL

K-Number: K022389 · 2003-05-06

ApplicantWorldwide Medical Technologies, LLC
Decision Date2003-05-06
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

READI-LOAD SYSTEM, MODEL PSS 1820RL is the device name listed in this FDA 510(k) record. The listed applicant is Worldwide Medical Technologies, LLC. It received FDA 510(k) clearance on 2003-05-06 under 510(k) number K022389. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the READI-LOAD SYSTEM, MODEL PSS 1820RL?

READI-LOAD SYSTEM, MODEL PSS 1820RL is a medical device that received FDA 510(k) clearance on 2003-05-06. The listed applicant is Worldwide Medical Technologies, LLC. The 510(k) number is K022389.

When did READI-LOAD SYSTEM, MODEL PSS 1820RL receive FDA 510(k) clearance?

READI-LOAD SYSTEM, MODEL PSS 1820RL received FDA 510(k) clearance on 2003-05-06, under 510(k) number K022389.

Who is the listed applicant for READI-LOAD SYSTEM, MODEL PSS 1820RL?

The FDA 510(k) record lists Worldwide Medical Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for READI-LOAD SYSTEM, MODEL PSS 1820RL?

The FDA product code for READI-LOAD SYSTEM, MODEL PSS 1820RL is KXK.

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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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