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FDA 510(k)

B-GCG SYSTEM BY RIA

K-Number: K830526 · 1983-04-05

ApplicantPcl-Ria, Inc.
Decision Date1983-04-05
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

B-GCG SYSTEM BY RIA is the device name listed in this FDA 510(k) record. The listed applicant is Pcl-Ria, Inc.. It received FDA 510(k) clearance on 1983-04-05 under 510(k) number K830526. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B-GCG SYSTEM BY RIA?

B-GCG SYSTEM BY RIA is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is Pcl-Ria, Inc.. The 510(k) number is K830526.

When did B-GCG SYSTEM BY RIA receive FDA 510(k) clearance?

B-GCG SYSTEM BY RIA received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830526.

Who is the listed applicant for B-GCG SYSTEM BY RIA?

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

What is the FDA product code for B-GCG SYSTEM BY RIA?

The FDA product code for B-GCG SYSTEM BY RIA is JHI.

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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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