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FDA 510(k)

SDL-10 DIAGNOSTIC ULTRASOUND

K-Number: K837314 · 1983-04-29

ApplicantShimadzu Corp.
Decision Date1983-04-29
Product Code
DecisionSubstantially Equivalent

Device Summary

SDL-10 DIAGNOSTIC ULTRASOUND is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corp.. It received FDA 510(k) clearance on 1983-04-29 under 510(k) number K837314. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SDL-10 DIAGNOSTIC ULTRASOUND?

SDL-10 DIAGNOSTIC ULTRASOUND is a medical device that received FDA 510(k) clearance on 1983-04-29. The listed applicant is Shimadzu Corp.. The 510(k) number is K837314.

When did SDL-10 DIAGNOSTIC ULTRASOUND receive FDA 510(k) clearance?

SDL-10 DIAGNOSTIC ULTRASOUND received FDA 510(k) clearance on 1983-04-29, under 510(k) number K837314.

Who is the listed applicant for SDL-10 DIAGNOSTIC ULTRASOUND?

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

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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-300K101036SHIMADZU COLLIMATOR R-20JK090578SHIMADZU COLLIMATOR R-30HK090268SHIMADZU MOBILE X-RAY SYSTEM MOBILE ART EVOLUTIONK080701SHIMADZU MOBILE X-RAY SYSTEM MOBILEDART EVOLUTIONK072006DAR-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.

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