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FDA 510(k)

SARNS NON-FILTERED VENOUS RESERVOIR

K-Number: K912915 · 1991-09-25

Applicant3M Health Care, Ltd.
Decision Date1991-09-25
Product CodeDTP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS NON-FILTERED VENOUS RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Ltd.. It received FDA 510(k) clearance on 1991-09-25 under 510(k) number K912915. 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 NON-FILTERED VENOUS RESERVOIR?

SARNS NON-FILTERED VENOUS RESERVOIR is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K912915.

When did SARNS NON-FILTERED VENOUS RESERVOIR receive FDA 510(k) clearance?

SARNS NON-FILTERED VENOUS RESERVOIR received FDA 510(k) clearance on 1991-09-25, under 510(k) number K912915.

Who is the listed applicant for SARNS NON-FILTERED VENOUS RESERVOIR?

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

What is the FDA product code for SARNS NON-FILTERED VENOUS RESERVOIR?

The FDA product code for SARNS NON-FILTERED VENOUS RESERVOIR is DTP.

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Other records listing 3M Health Care, Ltd. 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.

K953904SARNS 9000 UNIVERSAL ROLLER PUMPK926364ATTEST BRAND RAPID READOUT BIOLOGICAL IND. #129XK941534MODULAR VS-22 CEMENTED FEMORAL HIP SYSTEMK941748STERI-VAC GAS STERILIZER MODEL 8XLK9306813M PREVENTION FABRIC SURGICAL GOWN #78XXK9323073M MAXI-DRIVER II DBATTERY POWERED SYSTEM

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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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