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FDA 510(k)

DSL 1600

K-Number: K822898 · 1982-12-09

Decision Date1982-12-09
Product CodeCIA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DSL 1600 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 1982-12-09 under 510(k) number K822898. The device is classified under product code CIA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSL 1600?

DSL 1600 is a medical device that received FDA 510(k) clearance on 1982-12-09. The listed applicant is Diagnostic Systems Laboratories, Inc.. The 510(k) number is K822898.

When did DSL 1600 receive FDA 510(k) clearance?

DSL 1600 received FDA 510(k) clearance on 1982-12-09, under 510(k) number K822898.

Who is the listed applicant for DSL 1600?

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 DSL 1600?

The FDA product code for DSL 1600 is CIA.

Other records listing Diagnostic Systems 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.

View all 94 devices →

Related Devices (Code: CIA)

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.

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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