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FDA 510(k)

CATHETER EXTENSION SET CAT. NO. 48-3027-9

K-Number: K895992 · 1990-03-23

Decision Date1990-03-23
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER EXTENSION SET CAT. NO. 48-3027-9 is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Care, Medical Products Div., Inc.. It received FDA 510(k) clearance on 1990-03-23 under 510(k) number K895992. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER EXTENSION SET CAT. NO. 48-3027-9?

CATHETER EXTENSION SET CAT. NO. 48-3027-9 is a medical device that received FDA 510(k) clearance on 1990-03-23. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K895992.

When did CATHETER EXTENSION SET CAT. NO. 48-3027-9 receive FDA 510(k) clearance?

CATHETER EXTENSION SET CAT. NO. 48-3027-9 received FDA 510(k) clearance on 1990-03-23, under 510(k) number K895992.

Who is the listed applicant for CATHETER EXTENSION SET CAT. NO. 48-3027-9?

The FDA 510(k) record lists National Medical Care, Medical Products Div., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER EXTENSION SET CAT. NO. 48-3027-9?

The FDA product code for CATHETER EXTENSION SET CAT. NO. 48-3027-9 is KDJ.

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 National Medical Care, Medical Products Div., 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.

View all 62 devices →

Related Devices (Code: KDJ)

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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