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FDA 510(k)

NEO-PICC

K-Number: K970434 · 1997-04-01

Decision Date1997-04-01
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEO-PICC is the device name listed in this FDA 510(k) record. The listed applicant is Klein-Baker Medical, Inc.. It received FDA 510(k) clearance on 1997-04-01 under 510(k) number K970434. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEO-PICC?

NEO-PICC is a medical device that received FDA 510(k) clearance on 1997-04-01. The listed applicant is Klein-Baker Medical, Inc.. The 510(k) number is K970434.

When did NEO-PICC receive FDA 510(k) clearance?

NEO-PICC received FDA 510(k) clearance on 1997-04-01, under 510(k) number K970434.

Who is the listed applicant for NEO-PICC?

The FDA 510(k) record lists Klein-Baker Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEO-PICC?

The FDA product code for NEO-PICC is LJS.

Other records listing Klein-Baker Medical, Inc. 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: LJS)

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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