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FDA 510(k)

COBE/STOCKERT BATTERY MODULE

K-Number: K802714 · 1980-11-26

ApplicantCobe Laboratories, Inc.
Decision Date1980-11-26
Product CodeDWB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COBE/STOCKERT BATTERY MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Cobe Laboratories, Inc.. It received FDA 510(k) clearance on 1980-11-26 under 510(k) number K802714. The device is classified under product code DWB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COBE/STOCKERT BATTERY MODULE?

COBE/STOCKERT BATTERY MODULE is a medical device that received FDA 510(k) clearance on 1980-11-26. The listed applicant is Cobe Laboratories, Inc.. The 510(k) number is K802714.

When did COBE/STOCKERT BATTERY MODULE receive FDA 510(k) clearance?

COBE/STOCKERT BATTERY MODULE received FDA 510(k) clearance on 1980-11-26, under 510(k) number K802714.

Who is the listed applicant for COBE/STOCKERT BATTERY MODULE?

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

What is the FDA product code for COBE/STOCKERT BATTERY MODULE?

The FDA product code for COBE/STOCKERT BATTERY MODULE is DWB.

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Other records listing Cobe Laboratories, 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.

K923272COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATORK900105COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTICK905793COBE CENTRY 2 BICART OPTION KITK905388COBE CENTRYSYSTEM 3 BICART OPTION KITK904336NEW COBE SATURATION/HEMATOCRIT MONITORK902631COBE ICU CONVERSION KIT

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Related Devices (Code: DWB)

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.

K162843Small (4) Roller Pump for the Terumo Advanced Perfusion System 1, Large (6) Roller Pump for the Terumo Advanced Perfusion System 1Terumo Cardiovascular Systems CorporationK131618LARGE (6) ROLLER PUMP FOR TERUMO ADVANCED PERFUSION SYSTEM 1; LARGE (6) ROLLER PUMP FOR TERUMO ADVANCED PERFUSION SYSTTerumo Cardiovascular Systems CorporationK112587ADVANCED PERFUSION SYSTEM 1 (APS1) TUBE CLAMP ASSEMBLY, ROLLER PUMP 6 INCH CLASSIC COLOR,Terumo Cardiovascular Systems Corp.K973237CSS-CARDIOPLEGIA SAFETY SYSTEMMedtronic Bio-Medicus, Inc.K972321S3 MAST PUMPStoeckert InstrumenteK971520S3 CYCLIC RPM CONTROLStoeckert Instrumente

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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