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FDA 510(k)

DIDECO VACUUM PUMP

K-Number: K936220 · 1995-01-27

ApplicantDideco
Decision Date1995-01-27
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DIDECO VACUUM PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Dideco. It received FDA 510(k) clearance on 1995-01-27 under 510(k) number K936220. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIDECO VACUUM PUMP?

DIDECO VACUUM PUMP is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is Dideco. The 510(k) number is K936220.

When did DIDECO VACUUM PUMP receive FDA 510(k) clearance?

DIDECO VACUUM PUMP received FDA 510(k) clearance on 1995-01-27, under 510(k) number K936220.

Who is the listed applicant for DIDECO VACUUM PUMP?

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

What is the FDA product code for DIDECO VACUUM PUMP?

The FDA product code for DIDECO VACUUM PUMP is CAC.

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 Dideco 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.

K004001MONOLYTH MIMESYS HOLLOW FIBER OXYGENATORK010478DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS RESERVOIR BAG, WITH BIOCOMPATABLE TREATMENT SURK001388DATA MASTER PERFUSION MONITORING SYSTEMK940519DIDECO COMPACT-A AUTOTRANSFUSION SYSTEM

Related Devices (Code: CAC)

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.

K241236XTRA Collection sets; XTRA Sequestration set XSorin Group Italia S.R.L.K240426Aventus Clot Management SystemInquis MedicalK240584XTRA Autotransfusion System (with XTRA Bowl sets)Sorin Group Italia S.R.L.K231782FlowSaver Blood Return System (80-101)Inari Medical, Inc.K221483FlowSaver Blood Return SystemInari Medical, Inc.K221722Haemonetics Cell Saver Elite/Elite+ Autotransfusion System (CSE-E-US/CSE-EW-US)Haemonetics Corporation

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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