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FDA 510(k)

ERIKA ARTERIAL LINE 03-9625-9

K-Number: K860740 · 1986-03-14

ApplicantNational Medical Care, Medical Products Div., Inc.
Decision Date1986-03-14
Product CodeFJK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ERIKA ARTERIAL LINE 03-9625-9 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 1986-03-14 under 510(k) number K860740. The device is classified under product code FJK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERIKA ARTERIAL LINE 03-9625-9?

ERIKA ARTERIAL LINE 03-9625-9 is a medical device that received FDA 510(k) clearance on 1986-03-14. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K860740.

When did ERIKA ARTERIAL LINE 03-9625-9 receive FDA 510(k) clearance?

ERIKA ARTERIAL LINE 03-9625-9 received FDA 510(k) clearance on 1986-03-14, under 510(k) number K860740.

Who is the listed applicant for ERIKA ARTERIAL LINE 03-9625-9?

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 ERIKA ARTERIAL LINE 03-9625-9?

The FDA product code for ERIKA ARTERIAL LINE 03-9625-9 is FJK.

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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.

K962081COMBILINES HEMODIALYSIS BLOOD TUBING SETK941757FORMALIN REUSE CARTK952343FOCUA 90R, 90HR, 120R, 120HR, 160R, 160HR HOLLOW FIBER DIALYZERK930843RAPID DISCONNECT Y-SET, CAT. NO. 48-7000K914790HOLLOW FIBER DIALYZER FOCUS 9OR/90H-R/120R/120H-RK920697DEXTROLYTE II PERITONEAL DIALYSIS 48-3029-7 CLAMP

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Related Devices (Code: FJK)

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.

K252423NovaLine Tubing Set for Hemodialysis (BL 124)Bain Medical Equipment (Guangzhou) Co., Ltd.K251341VITAL Tubing Sets for HemodialysisVital Healthcare Sdn. Bhd.K251442TIANYI Extracorporeal Blood Tubing Set (TY-NDEO-A1)Ningbo Tianyi Medical Appliance Co., Ltd.K243607Moda-flx Hemodialysis System™ Cartridge (102121-001 )Diality, Inc.K213992CombiSet Hemodialysis Blood Tubing SetFresenius Medical Care Renal Therapies Group, LLCK210782Tablo CartridgeOutset Medical, Inc.

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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