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FDA 510(k)

PS MEDICAL IPI ACCESS KIT

K-Number: K930206 · 1994-02-25

Decision Date1994-02-25
Product CodeLJT
Advisory CommitteeHO
DecisionUnknown

Device Summary

PS MEDICAL IPI ACCESS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Pudenz-Schulte Medical Research Corp.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K930206. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PS MEDICAL IPI ACCESS KIT?

PS MEDICAL IPI ACCESS KIT is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Pudenz-Schulte Medical Research Corp.. The 510(k) number is K930206.

When did PS MEDICAL IPI ACCESS KIT receive FDA 510(k) clearance?

PS MEDICAL IPI ACCESS KIT received FDA 510(k) clearance on 1994-02-25, under 510(k) number K930206.

Who is the listed applicant for PS MEDICAL IPI ACCESS KIT?

The FDA 510(k) record lists Pudenz-Schulte Medical Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PS MEDICAL IPI ACCESS KIT?

The FDA product code for PS MEDICAL IPI ACCESS KIT is LJT.

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 Pudenz-Schulte Medical Research Corp. 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.

View all 40 devices →

Related Devices (Code: LJT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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