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FDA 510(k)

SIGMA 20 ELECTRONIC SECTOR SCANNER

K-Number: K833680 · 1984-02-17

ApplicantKontron Instruments, Inc.
Decision Date1984-02-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIGMA 20 ELECTRONIC SECTOR SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Kontron Instruments, Inc.. It received FDA 510(k) clearance on 1984-02-17 under 510(k) number K833680. 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 SIGMA 20 ELECTRONIC SECTOR SCANNER?

SIGMA 20 ELECTRONIC SECTOR SCANNER is a medical device that received FDA 510(k) clearance on 1984-02-17. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K833680.

When did SIGMA 20 ELECTRONIC SECTOR SCANNER receive FDA 510(k) clearance?

SIGMA 20 ELECTRONIC SECTOR SCANNER received FDA 510(k) clearance on 1984-02-17, under 510(k) number K833680.

Who is the listed applicant for SIGMA 20 ELECTRONIC SECTOR SCANNER?

The FDA 510(k) record lists Kontron Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIGMA 20 ELECTRONIC SECTOR SCANNER?

The FDA product code for SIGMA 20 ELECTRONIC SECTOR SCANNER is IYO.

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Other records listing Kontron Instruments, Inc. as applicant

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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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