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FDA 510(k)

SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908

K-Number: K961155 · 1996-06-18

Decision Date1996-06-18
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908 is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Medical Products Corp.. It received FDA 510(k) clearance on 1996-06-18 under 510(k) number K961155. 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 SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908?

SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908 is a medical device that received FDA 510(k) clearance on 1996-06-18. The listed applicant is Douglas Medical Products Corp.. The 510(k) number is K961155.

When did SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908 receive FDA 510(k) clearance?

SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908 received FDA 510(k) clearance on 1996-06-18, under 510(k) number K961155.

Who is the listed applicant for SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908?

The FDA 510(k) record lists Douglas Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908?

The FDA product code for SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908 is LJS.

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 Douglas Medical Products 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 19 devices →

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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