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FDA 510(k)

GLUCAGON RIA MODULE

K-Number: K771948 · 1978-01-20

ApplicantInter Science Institute
Decision Date1978-01-20
Product CodeJME
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCAGON RIA MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Inter Science Institute. It received FDA 510(k) clearance on 1978-01-20 under 510(k) number K771948. The device is classified under product code JME. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUCAGON RIA MODULE?

GLUCAGON RIA MODULE is a medical device that received FDA 510(k) clearance on 1978-01-20. The listed applicant is Inter Science Institute. The 510(k) number is K771948.

When did GLUCAGON RIA MODULE receive FDA 510(k) clearance?

GLUCAGON RIA MODULE received FDA 510(k) clearance on 1978-01-20, under 510(k) number K771948.

Who is the listed applicant for GLUCAGON RIA MODULE?

The FDA 510(k) record lists Inter Science Institute as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLUCAGON RIA MODULE?

The FDA product code for GLUCAGON RIA MODULE is JME.

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 Inter Science Institute 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.

K771953GASTRIN RIA MODULEK771947INSULIN RIA MODULE

Related Devices (Code: JME)

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.

K893975DOUBLE ANTIBODY GLUCAGONDiagnostic Products Corp.K782143RIA KIT, GLUCOSESerono 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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