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FDA 510(k)

RIA SSIST TI-59 MAGNETIC CARD PROGRAMS

K-Number: K822860 · 1982-10-27

ApplicantVentrex Laboratories, Inc.
Decision Date1982-10-27
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA SSIST TI-59 MAGNETIC CARD PROGRAMS is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1982-10-27 under 510(k) number K822860. 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 RIA SSIST TI-59 MAGNETIC CARD PROGRAMS?

RIA SSIST TI-59 MAGNETIC CARD PROGRAMS is a medical device that received FDA 510(k) clearance on 1982-10-27. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K822860.

When did RIA SSIST TI-59 MAGNETIC CARD PROGRAMS receive FDA 510(k) clearance?

RIA SSIST TI-59 MAGNETIC CARD PROGRAMS received FDA 510(k) clearance on 1982-10-27, under 510(k) number K822860.

Who is the listed applicant for RIA SSIST TI-59 MAGNETIC CARD PROGRAMS?

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

What is the FDA product code for RIA SSIST TI-59 MAGNETIC CARD PROGRAMS?

The FDA product code for RIA SSIST TI-59 MAGNETIC CARD PROGRAMS is JQP.

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Other records listing Ventrex 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.

K914554SPECIFIC IGE EIA-TURBO ASSAYK913833VENTREX ALLERGEN DISCK913434VENTREX COATED TUBE INTACT PTHK905612VENTREX COATED TUBE IGE RADIOIMMUNOASSAYK905636VENTREX COATED TUBE IGE ENZYME IMMUNOASSAYK905247SHBG IRMA KIT

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Related Devices (Code: JQP)

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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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