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FDA 510(k)

MODEL LS 3000 LINEAR SCANNER

K-Number: K827377 · 1982-07-13

ApplicantHitachi Medical Corp.
Decision Date1982-07-13
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL LS 3000 LINEAR SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Hitachi Medical Corp.. It received FDA 510(k) clearance on 1982-07-13 under 510(k) number K827377. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL LS 3000 LINEAR SCANNER?

MODEL LS 3000 LINEAR SCANNER is a medical device that received FDA 510(k) clearance on 1982-07-13. The listed applicant is Hitachi Medical Corp.. The 510(k) number is K827377.

When did MODEL LS 3000 LINEAR SCANNER receive FDA 510(k) clearance?

MODEL LS 3000 LINEAR SCANNER received FDA 510(k) clearance on 1982-07-13, under 510(k) number K827377.

Who is the listed applicant for MODEL LS 3000 LINEAR SCANNER?

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

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Other records listing Hitachi Medical 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.

K073310OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COILK061608MODIFICATION TO EUB-5500 DIAGNOSTIC ULTRASOUND SCANNERK053258EUB-6500 DIAGNOSTIC ULTRASOUND SCANNERK042501ETG-4000 OPTICAL TOPOGRAPHY SYSTEMK013722MODIFICATION TO: EUB-8500 DIAGNOSTIC ULTRASOUND SCANNERK013723MODIFICATION TO: EUB-6500 DIAGNOSTIC ULTRASOUND SCANNER

View all 11 devices →

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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