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FDA 510(k)

ACTH RIA SYSTEM-DSI 2300

K-Number: K830893 · 1983-04-27

ApplicantDiagnostic Systems Laboratories, Inc.
Decision Date1983-04-27
Product CodeCKG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACTH RIA SYSTEM-DSI 2300 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Systems Laboratories, Inc.. It received FDA 510(k) clearance on 1983-04-27 under 510(k) number K830893. The device is classified under product code CKG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTH RIA SYSTEM-DSI 2300?

ACTH RIA SYSTEM-DSI 2300 is a medical device that received FDA 510(k) clearance on 1983-04-27. The listed applicant is Diagnostic Systems Laboratories, Inc.. The 510(k) number is K830893.

When did ACTH RIA SYSTEM-DSI 2300 receive FDA 510(k) clearance?

ACTH RIA SYSTEM-DSI 2300 received FDA 510(k) clearance on 1983-04-27, under 510(k) number K830893.

Who is the listed applicant for ACTH RIA SYSTEM-DSI 2300?

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

What is the FDA product code for ACTH RIA SYSTEM-DSI 2300?

The FDA product code for ACTH RIA SYSTEM-DSI 2300 is CKG.

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Related Devices (Code: CKG)

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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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