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FDA 510(k)

STERICAP ASSEMBLY AND REPLACEMENT TRAY

K-Number: K872067 · 1987-08-04

ApplicantStericap Systems
Decision Date1987-08-04
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERICAP ASSEMBLY AND REPLACEMENT TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Stericap Systems. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K872067. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERICAP ASSEMBLY AND REPLACEMENT TRAY?

STERICAP ASSEMBLY AND REPLACEMENT TRAY is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is Stericap Systems. The 510(k) number is K872067.

When did STERICAP ASSEMBLY AND REPLACEMENT TRAY receive FDA 510(k) clearance?

STERICAP ASSEMBLY AND REPLACEMENT TRAY received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872067.

Who is the listed applicant for STERICAP ASSEMBLY AND REPLACEMENT TRAY?

The FDA 510(k) record lists Stericap Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERICAP ASSEMBLY AND REPLACEMENT TRAY?

The FDA product code for STERICAP ASSEMBLY AND REPLACEMENT TRAY is FMG.

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 Stericap Systems 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.

K872066STERICAP STOPCOCK

Related Devices (Code: FMG)

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.

K242255Qitexio® 4-Way Stopcock (QIT014)MedexK223499Three Way Stop CockM/S Romsons InternationalK223175lntravascular Administration Sets with Stopcock and ManifoldBaxter Healthcare CorporationK211204SafePort(TM) Manifold (or Stopcock)Elcam Medical AcalK210516Clicky CrossYomura Technologies, Inc.K190539TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non SterileMonumedical, LLC

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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