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FDA 510(k)

AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR

K-Number: K915737 · 1992-09-03

ApplicantElectromedics, Inc.
Decision Date1992-09-03
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1992-09-03 under 510(k) number K915737. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR?

AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR is a medical device that received FDA 510(k) clearance on 1992-09-03. The listed applicant is Electromedics, Inc.. The 510(k) number is K915737.

When did AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR receive FDA 510(k) clearance?

AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR received FDA 510(k) clearance on 1992-09-03, under 510(k) number K915737.

Who is the listed applicant for AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR?

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

What is the FDA product code for AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR?

The FDA product code for AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR is DTN.

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Other records listing Electromedics, 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.

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Related Devices (Code: DTN)

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.

K251783Inspire HCR and HCR DUAL cardiotomy reservoirsSorin Group Italia S.R.L.K241206Quantum Perfusion Hybrid SystemSpectrum Medical S.R.L.K241053MVR™ Venous Reservoir Bag 800 mL; MVR™ Venous Reservoir Bag 1600 mL; MVR™ Venous Reservoir Bag with Cortiva™ BioActive Surface 800 mL; MVR™ Venous Reservoir Bag with Cortiva™ BioActive Surface 1600 mLMedtronic Cardiac SurgeryK223361BMR 1900 PHISIOSorin Group Italia S.R.L.K170583Intersept Filtered Cardiotomy Reservoir with Cortiva BioActive SurfaceMedtronic, Inc.K161733INSPIRE SVR 1200, INSPIRE 6F C, INSPIRE 8F CSorin Group Italia S.R.L.

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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