FDA 510(k)

DSL-150

K-Number: K840611 · 1984-04-20

Decision Date1984-04-20

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DSL-150 is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corp.. It received FDA 510(k) clearance on 1984-04-20 under 510(k) number K840611. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSL-150?

DSL-150 is a medical device that received FDA 510(k) clearance on 1984-04-20. The listed applicant is Shimadzu Corp.. The 510(k) number is K840611.

When did DSL-150 receive FDA 510(k) clearance?

DSL-150 received FDA 510(k) clearance on 1984-04-20, under 510(k) number K840611.

Who is the listed applicant for DSL-150?

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

What is the FDA product code for DSL-150?

The FDA product code for DSL-150 is IYO.

Other records listing Shimadzu Corp. 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.

K101039SHIMADZU COLLIMATOR R-300 K101036SHIMADZU COLLIMATOR R-20J K090578SHIMADZU COLLIMATOR R-30H K090268SHIMADZU MOBILE X-RAY SYSTEM MOBILE ART EVOLUTION K080701SHIMADZU MOBILE X-RAY SYSTEM MOBILEDART EVOLUTION K072006DAR-9400F

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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.