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FDA 510(k)

SARNS FILTERED CARDIOTOMY RESERVOIR

K-Number: K860702 · 1986-05-28

Applicant3M Health Care, Sarns
Decision Date1986-05-28
Product CodeDTP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS FILTERED CARDIOTOMY RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Sarns. It received FDA 510(k) clearance on 1986-05-28 under 510(k) number K860702. The device is classified under product code DTP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNS FILTERED CARDIOTOMY RESERVOIR?

SARNS FILTERED CARDIOTOMY RESERVOIR is a medical device that received FDA 510(k) clearance on 1986-05-28. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K860702.

When did SARNS FILTERED CARDIOTOMY RESERVOIR receive FDA 510(k) clearance?

SARNS FILTERED CARDIOTOMY RESERVOIR received FDA 510(k) clearance on 1986-05-28, under 510(k) number K860702.

Who is the listed applicant for SARNS FILTERED CARDIOTOMY RESERVOIR?

The FDA 510(k) record lists 3M Health Care, Sarns as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SARNS FILTERED CARDIOTOMY RESERVOIR?

The FDA product code for SARNS FILTERED CARDIOTOMY RESERVOIR is DTP.

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Other records listing 3M Health Care, Sarns 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.

K960916SAMS 8000 CARDIOPLEGIA MONITORK953901SARNS 800 ROLLER PUMPK9507393M SARNS FLOW SENSOR, CENTRIFUGAL CONTROL MODULE 115, 220 V, 900 PERFUSION SYSTEMK941653SARNS TURBO MEMBRANE OXYGENATOR MODIFICATIONK941654SARNS FILTERED VENOUS RESERVIOR MODIFICATIONK940651SARNS ULTRASONIC AIR SENSOR

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Related Devices (Code: DTP)

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.

K101186AFFINITY VARD SUB-ASSEMBLY FOR CPS (CARMEDA COATED), PURGELINE (UNCOATED), HOLDING BAGMedtronic Perfusion SystemsK082412VENOUS BUBBLE TRAP, MODEL VBT 160; VENOUS BUBBLE TRAP WITH BIOLINE COATING, MODEL BE-VBT 160, BEQ-VBT 160Mapquet Cardiopulmonary AGK004046COBE VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR, COBE SMARXT VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIRCobe Cardiovascular, Inc.K002591COBE SMARXT VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIRCobe Cardiovascular, Inc.K990514MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VRC.R. Bard, Inc.K984322DIDECO D920, LILLIPUT 1 TWIN RESERVOIRDideco S.P.A.

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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