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FDA 510(k)

EL2-SERIES BLOOD COLLECTION REERVOIR

K-Number: K930154 · 1993-07-01

ApplicantElectromedics, Inc.
Decision Date1993-07-01
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EL2-SERIES BLOOD COLLECTION REERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1993-07-01 under 510(k) number K930154. 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 EL2-SERIES BLOOD COLLECTION REERVOIR?

EL2-SERIES BLOOD COLLECTION REERVOIR is a medical device that received FDA 510(k) clearance on 1993-07-01. The listed applicant is Electromedics, Inc.. The 510(k) number is K930154.

When did EL2-SERIES BLOOD COLLECTION REERVOIR receive FDA 510(k) clearance?

EL2-SERIES BLOOD COLLECTION REERVOIR received FDA 510(k) clearance on 1993-07-01, under 510(k) number K930154.

Who is the listed applicant for EL2-SERIES BLOOD COLLECTION REERVOIR?

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 EL2-SERIES BLOOD COLLECTION REERVOIR?

The FDA product code for EL2-SERIES BLOOD COLLECTION REERVOIR 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.

K934964ELECTROMEDICS TYMPANIC TEMPERATURE SENSORK933832ELECTROMEDICS HG (HYDROGEL) SERIES SKIN TEMPERATURE SENSORK934355ELECTROMEDICS BLOOD HEAT EXCHANGERK926250ELECTROMEDICS EL-SERIES CARDIOTOMY RESERVOIRK925412ELECTROMEDICS TISSUE TRAP/ #TT280K915737AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR

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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.

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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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