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FDA 510(k)

BLOOD CELL PROCESSOR MODEL 2 IBM 2991

K-Number: K760856 · 1977-01-10

ApplicantIntl. Business Machines
Decision Date1977-01-10
Product CodeGKT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BLOOD CELL PROCESSOR MODEL 2 IBM 2991 is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Business Machines. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K760856. The device is classified under product code GKT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD CELL PROCESSOR MODEL 2 IBM 2991?

BLOOD CELL PROCESSOR MODEL 2 IBM 2991 is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Intl. Business Machines. The 510(k) number is K760856.

When did BLOOD CELL PROCESSOR MODEL 2 IBM 2991 receive FDA 510(k) clearance?

BLOOD CELL PROCESSOR MODEL 2 IBM 2991 received FDA 510(k) clearance on 1977-01-10, under 510(k) number K760856.

Who is the listed applicant for BLOOD CELL PROCESSOR MODEL 2 IBM 2991?

The FDA 510(k) record lists Intl. Business Machines as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD CELL PROCESSOR MODEL 2 IBM 2991?

The FDA product code for BLOOD CELL PROCESSOR MODEL 2 IBM 2991 is GKT.

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Other records listing Intl. Business Machines 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.

K831004AUTOMATED 8400 BLOOD CELL SEPARATORK830163IBM 588 DIGITAL ECG ACQUISITION/ANALYSISK812355IBM 2991 BLOOD CELL PROCESSOR MOD. 1 & 2K810989IBM 5880 ACQUISITION & ANALYSIS CART TELK810988IBM 5885 DIGITAL ECG ACQUISITION CARTK772353EKG ACQUISITION & ANALYSIS CART

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Related Devices (Code: GKT)

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.

K200530AMICUS Separator SystemFresenius Kabi AGK162462AMICUS Separator System, AMICUS Separator System; RefurbishedFresenius Kabi USA,LlcK822521AUTOMATED BLOOD CELL SEPARATORCryosan, Inc.K820396AUTOMATED BLOOD CELL SEPAR. DISP. SFTWRPheragen Technology Corp.K801233CELLTRIFUGE IITravenol Laboratories, S.A.K791106STERILE, DISPOSABLE CENTRIFUGE BOWLTravenol Laboratories, S.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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