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FDA 510(k)

CENTRIA INSULIN RIA

K-Number: K791707 · 1979-10-17

ApplicantVentrex Laboratories, Inc.
Decision Date1979-10-17
Product CodeCFP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIA INSULIN RIA 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 1979-10-17 under 510(k) number K791707. The device is classified under product code CFP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIA INSULIN RIA?

CENTRIA INSULIN RIA is a medical device that received FDA 510(k) clearance on 1979-10-17. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K791707.

When did CENTRIA INSULIN RIA receive FDA 510(k) clearance?

CENTRIA INSULIN RIA received FDA 510(k) clearance on 1979-10-17, under 510(k) number K791707.

Who is the listed applicant for CENTRIA INSULIN RIA?

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 CENTRIA INSULIN RIA?

The FDA product code for CENTRIA INSULIN RIA is CFP.

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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.

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Related Devices (Code: CFP)

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.

K963911ALPCO/MERCODIA INSULIN ELISAAmerican Laboratory Products Co., Ltd.K953084ACCESS ULTRASENSITIVE INSULIN ASSAYBio-Rad Laboratories, Inc.K920109IMX INSULINAbbott LaboratoriesK914820DSL INSULIN RIA (DSL 1600)Diagnostic Systems Laboratories, Inc.K903628AIA-PACK IRITosoh Corp.K901135ENZYMUN TEST(R) INSULINBoehringer Mannheim Corp.

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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