FDA 510(k)

SIMPLAMATIC III

K-Number: K827450 · 1982-05-19

Decision Date1982-05-19

Product Code

DecisionSubstantially Equivalent

Device Summary

SIMPLAMATIC III is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum X-Ray Corp.. It received FDA 510(k) clearance on 1982-05-19 under 510(k) number K827450. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMPLAMATIC III?

SIMPLAMATIC III is a medical device that received FDA 510(k) clearance on 1982-05-19. The listed applicant is Spectrum X-Ray Corp.. The 510(k) number is K827450.

When did SIMPLAMATIC III receive FDA 510(k) clearance?

SIMPLAMATIC III received FDA 510(k) clearance on 1982-05-19, under 510(k) number K827450.

Who is the listed applicant for SIMPLAMATIC III?

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

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Other records listing Spectrum X-Ray Corp. as applicant

K933134SPECTRUM DG-P7000 PEDIATRIC CRADLE K931563SPECTRUM MARK I SPECIAL PROCEDURES TABLE K870707PENTAMAX 1 MODEL B TABLE SYSTEM K840463DIGITAL CRADLE K834494SPECTRUM X-RAY CORP K813561SPECTRUM PEDIATRIC CARDLE TABLE

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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.