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FDA 510(k)

K 750 COMPUTER/DATA PROCESSOR

K-Number: K801091 · 1980-06-09

ApplicantJ.T. Baker Chemical Co.
Decision Date1980-06-09
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

K 750 COMPUTER/DATA PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is J.T. Baker Chemical Co.. It received FDA 510(k) clearance on 1980-06-09 under 510(k) number K801091. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K 750 COMPUTER/DATA PROCESSOR?

K 750 COMPUTER/DATA PROCESSOR is a medical device that received FDA 510(k) clearance on 1980-06-09. The listed applicant is J.T. Baker Chemical Co.. The 510(k) number is K801091.

When did K 750 COMPUTER/DATA PROCESSOR receive FDA 510(k) clearance?

K 750 COMPUTER/DATA PROCESSOR received FDA 510(k) clearance on 1980-06-09, under 510(k) number K801091.

Who is the listed applicant for K 750 COMPUTER/DATA PROCESSOR?

The FDA 510(k) record lists J.T. Baker Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K 750 COMPUTER/DATA PROCESSOR?

The FDA product code for K 750 COMPUTER/DATA PROCESSOR is JQP.

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Other records listing J.T. Baker Chemical Co. 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.

K803128SERIES 810 PLATELET ANALYZERK802080BAKER DIAG. ULTRARATE CHLORIDE KITK801909LSA 290 ASSAY REAGENTS/NEPHELOMETRICK802035BAKER DIAG. ULTRARATE CO2 REAGENT KITK801795BAKER DIAGNOSTIC ULTRA-RATE SODIUM/POT.K801661J.T. BAKER CERULOPLASMIN NEPHELOMETRIC

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Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, Inc.

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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