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FDA 510(k)

INTERSEPT* OXYGEN GAS LINE FILTER

K-Number: K882136 · 1988-08-11

ApplicantMedtronic Blood Systems, Inc.
Decision Date1988-08-11
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERSEPT* OXYGEN GAS LINE FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Blood Systems, Inc.. It received FDA 510(k) clearance on 1988-08-11 under 510(k) number K882136. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSEPT* OXYGEN GAS LINE FILTER?

INTERSEPT* OXYGEN GAS LINE FILTER is a medical device that received FDA 510(k) clearance on 1988-08-11. The listed applicant is Medtronic Blood Systems, Inc.. The 510(k) number is K882136.

When did INTERSEPT* OXYGEN GAS LINE FILTER receive FDA 510(k) clearance?

INTERSEPT* OXYGEN GAS LINE FILTER received FDA 510(k) clearance on 1988-08-11, under 510(k) number K882136.

Who is the listed applicant for INTERSEPT* OXYGEN GAS LINE FILTER?

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

What is the FDA product code for INTERSEPT* OXYGEN GAS LINE FILTER?

The FDA product code for INTERSEPT* OXYGEN GAS LINE FILTER is KRD.

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Other records listing Medtronic Blood Systems, Inc. as applicant

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K944966UNIPOLAR ATRIAL TEMPORARY PACING LEAD,MODEL 6492K944957TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500K893207CLOSED CHEST SUPPORT CIRCUITK893678DURAN FLEXIBLE ANNULOPLASTY RING & OBTURATOR H601HK891687EXTRACORPOREAL CIRCUIT WITH BIO-ACTIVE SURFACEK891230MAXIMA* HOLLOW FIBER OXYGENATOR W/FILTERED RESERV.

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Related Devices (Code: KRD)

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.

K252812UniPearls® Embolic MicrospheresSuzhou Haowei Medical Technology Co., Ltd.K261488OBSIDIO Conformable EmbolicBoston Scientific CorporationK261866Concerto Versa™ Detachable CoilMedtronic, Inc.K260635HARBOR Occlusion DeviceNuvascular, Inc.K260508LOBO Vascular Occlusion SystemOkami Medical, Inc.K253511Concerto Versa™ Detachable CoilMedtronic, 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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