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FDA 510(k)

MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER

K-Number: K880671 · 1988-05-06

ApplicantMedtronic Blood Systems, Inc.
Decision Date1988-05-06
Product CodeDTM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED INTERSEPT PEDIATRIC BLOOD 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 1988-05-06 under 510(k) number K880671. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER?

MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Medtronic Blood Systems, Inc.. The 510(k) number is K880671.

When did MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER receive FDA 510(k) clearance?

MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER received FDA 510(k) clearance on 1988-05-06, under 510(k) number K880671.

Who is the listed applicant for MODIFIED INTERSEPT PEDIATRIC BLOOD 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 MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER?

The FDA product code for MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER is DTM.

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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: DTM)

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.

K251744Affinity Pixie™ Arterial Filter with Balance™ Biosurface; Affinity® Pediatric Arterial Blood FilterMedtronicK242953KIDS Arterial FiltersSorin Group Italia S.R.L.K242092MICRO Arterial FiltersSorin Group Italia S.R.L.K231362OCS Heart Leukocyte Depleting FilterTransMedics, Inc.K123351AFFINITY AF100 ARTERIAL FILTER WITH CARMEDA BIOACTIVE SURFACEMedtronic Perfusion SystemsK122760AFFINITY AF100 ARTERIAL FILTER WITH BALANCE BIOSURFACEMedtronic, 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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