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FDA 510(k)

JSZ-MULTIPURPOSE SOLUTION

K-Number: K050517 · 2005-04-13

Decision Date2005-04-13
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

JSZ-MULTIPURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Szabocsik and Associates. It received FDA 510(k) clearance on 2005-04-13 under 510(k) number K050517. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JSZ-MULTIPURPOSE SOLUTION?

JSZ-MULTIPURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 2005-04-13. The listed applicant is Szabocsik and Associates. The 510(k) number is K050517.

When did JSZ-MULTIPURPOSE SOLUTION receive FDA 510(k) clearance?

JSZ-MULTIPURPOSE SOLUTION received FDA 510(k) clearance on 2005-04-13, under 510(k) number K050517.

Who is the listed applicant for JSZ-MULTIPURPOSE SOLUTION?

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

What is the FDA product code for JSZ-MULTIPURPOSE SOLUTION?

The FDA product code for JSZ-MULTIPURPOSE SOLUTION is LPN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Szabocsik and Associates as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LPN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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