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FDA 510(k)

LYRIS MODULAR INFO SYSTEM

K-Number: K831830 · 1984-06-25

ApplicantBiovation, Inc.
Decision Date1984-06-25
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LYRIS MODULAR INFO 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 1984-06-25 under 510(k) number K831830. 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 LYRIS MODULAR INFO SYSTEM?

LYRIS MODULAR INFO SYSTEM is a medical device that received FDA 510(k) clearance on 1984-06-25. The listed applicant is Biovation, Inc.. The 510(k) number is K831830.

When did LYRIS MODULAR INFO SYSTEM receive FDA 510(k) clearance?

LYRIS MODULAR INFO SYSTEM received FDA 510(k) clearance on 1984-06-25, under 510(k) number K831830.

Who is the listed applicant for LYRIS MODULAR INFO 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 LYRIS MODULAR INFO SYSTEM?

The FDA product code for LYRIS MODULAR INFO 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 BOARDK853026BIOVATION MAX DATA MANAGEMENT SYSTEMK842401CHEMISTRY CONSOLEK821534HEMATOLOGY 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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