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FDA 510(k)

SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER

K-Number: K873674 · 1988-10-07

ApplicantShimadzu Corp.
Decision Date1988-10-07
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corp.. It received FDA 510(k) clearance on 1988-10-07 under 510(k) number K873674. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER?

SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER is a medical device that received FDA 510(k) clearance on 1988-10-07. The listed applicant is Shimadzu Corp.. The 510(k) number is K873674.

When did SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER receive FDA 510(k) clearance?

SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER received FDA 510(k) clearance on 1988-10-07, under 510(k) number K873674.

Who is the listed applicant for SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER?

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 SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER?

The FDA product code for SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER is JOP.

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Other records listing Shimadzu Corp. as applicant

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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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Related Devices (Code: JOP)

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.

K242662Falcon/Xpress (Falcon/Xpress)Viasonix , Ltd.K233976VasoGuard (V10, V8, V6, V4, V2)Corvascular Diagnostics, LLCK153762Smartdop XT6Koven Technology, Inc.K131860VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDINGUs Vascular, LLCK111416FALCONViasonix , Ltd.K071730STUDIODOP VICORDERSkidmore Medical, Limited

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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