NP MEDICAL CAPLESS LUER ACTIVATED VALVE
K-Number: K973916 · 1998-03-09
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Device Summary
Frequently Asked Questions
What is the NP MEDICAL CAPLESS LUER ACTIVATED VALVE?
NP MEDICAL CAPLESS LUER ACTIVATED VALVE is a medical device that received FDA 510(k) clearance on 1998-03-09. The listed applicant is Np Medical, Inc.. The 510(k) number is K973916.
When did NP MEDICAL CAPLESS LUER ACTIVATED VALVE receive FDA 510(k) clearance?
NP MEDICAL CAPLESS LUER ACTIVATED VALVE received FDA 510(k) clearance on 1998-03-09, under 510(k) number K973916.
Who is the listed applicant for NP MEDICAL CAPLESS LUER ACTIVATED VALVE?
The FDA 510(k) record lists Np Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NP MEDICAL CAPLESS LUER ACTIVATED VALVE?
The FDA product code for NP MEDICAL CAPLESS LUER ACTIVATED VALVE is FPA.
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 Np 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: FPA)
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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