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FDA 510(k)

BIOVATION MAX DATA MANAGEMENT SYSTEM

K-Number: K853026 · 1985-08-02

ApplicantBiovation, Inc.
Decision Date1985-08-02
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BIOVATION MAX DATA MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biovation, Inc.. It received FDA 510(k) clearance on 1985-08-02 under 510(k) number K853026. 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 BIOVATION MAX DATA MANAGEMENT SYSTEM?

BIOVATION MAX DATA MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1985-08-02. The listed applicant is Biovation, Inc.. The 510(k) number is K853026.

When did BIOVATION MAX DATA MANAGEMENT SYSTEM receive FDA 510(k) clearance?

BIOVATION MAX DATA MANAGEMENT SYSTEM received FDA 510(k) clearance on 1985-08-02, under 510(k) number K853026.

Who is the listed applicant for BIOVATION MAX DATA MANAGEMENT SYSTEM?

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

What is the FDA product code for BIOVATION MAX DATA MANAGEMENT SYSTEM?

The FDA product code for BIOVATION MAX DATA MANAGEMENT SYSTEM is JQP.

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.

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Other records listing Biovation, 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.

K925528BIOVATION K-MANAGERK923844LYRIS 100/120 LABORATORY INFORMATION SYSTEMK915071DIFFERENTIAL COUNTING BOARDK842401CHEMISTRY CONSOLEK831830LYRIS MODULAR INFO SYSTEMK821534HEMATOLOGY DATA MANAGEMENT SYS

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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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