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FDA 510(k)

CARDIOPLEGIA COOLING SYST. CCAS-2

K-Number: K802848 · 1980-12-11

Decision Date1980-12-11
Product CodeDTR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOPLEGIA COOLING SYST. CCAS-2 is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1980-12-11 under 510(k) number K802848. The device is classified under product code DTR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOPLEGIA COOLING SYST. CCAS-2?

CARDIOPLEGIA COOLING SYST. CCAS-2 is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K802848.

When did CARDIOPLEGIA COOLING SYST. CCAS-2 receive FDA 510(k) clearance?

CARDIOPLEGIA COOLING SYST. CCAS-2 received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802848.

Who is the listed applicant for CARDIOPLEGIA COOLING SYST. CCAS-2?

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

What is the FDA product code for CARDIOPLEGIA COOLING SYST. CCAS-2?

The FDA product code for CARDIOPLEGIA COOLING SYST. CCAS-2 is DTR.

Related Clinical Trials

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.

Other records listing Bentley 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.

View all 55 devices →

Related Devices (Code: DTR)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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