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FDA 510(k)

LP EXTENSION SETS

K-Number: K870416 · 1987-04-06

ApplicantNorth Coast Medi-Tek
Decision Date1987-04-06
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LP EXTENSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is North Coast Medi-Tek. It received FDA 510(k) clearance on 1987-04-06 under 510(k) number K870416. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LP EXTENSION SETS?

LP EXTENSION SETS is a medical device that received FDA 510(k) clearance on 1987-04-06. The listed applicant is North Coast Medi-Tek. The 510(k) number is K870416.

When did LP EXTENSION SETS receive FDA 510(k) clearance?

LP EXTENSION SETS received FDA 510(k) clearance on 1987-04-06, under 510(k) number K870416.

Who is the listed applicant for LP EXTENSION SETS?

The FDA 510(k) record lists North Coast Medi-Tek as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LP EXTENSION SETS?

The FDA product code for LP EXTENSION SETS is FPK.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing North Coast Medi-Tek 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.

K870419IVR-SP CUSTOM ANGIOGRAPHY TRAYK870420PTC-6 AND PTC-8 PERCUTANEOUS CHOLANGIOGRAPHYK870418MYA-1 AND MYT-1 MYELOGRAM TRAYK870417RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAYK854095BIOPSY TRAY I & II

Related Devices (Code: FPK)

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.

K131517MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBINGMedrad, Inc. / Bayer Medical Care, Inc.K063114DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVESCoeur, Inc.K063239LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526Hospira, Inc.K052431MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1Medtronic MinimedK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)E-Z-Em, Inc.K031808MEDRAD SWABBABLE VALVE TRANSFER SETMedrad, 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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