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FDA 510(k)

READI-STRAND, MODEL PSSTRAND

K-Number: K023179 · 2003-07-02

ApplicantWorldwide Medical Technologies, LLC
Decision Date2003-07-02
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

READI-STRAND, MODEL PSSTRAND 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 2003-07-02 under 510(k) number K023179. 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-STRAND, MODEL PSSTRAND?

READI-STRAND, MODEL PSSTRAND is a medical device that received FDA 510(k) clearance on 2003-07-02. The listed applicant is Worldwide Medical Technologies, LLC. The 510(k) number is K023179.

When did READI-STRAND, MODEL PSSTRAND receive FDA 510(k) clearance?

READI-STRAND, MODEL PSSTRAND received FDA 510(k) clearance on 2003-07-02, under 510(k) number K023179.

Who is the listed applicant for READI-STRAND, MODEL PSSTRAND?

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-STRAND, MODEL PSSTRAND?

The FDA product code for READI-STRAND, MODEL PSSTRAND is KXK.

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Other records listing Worldwide Medical Technologies, LLC as applicant

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Related Devices (Code: 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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