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FDA 510(k)

MICRON-SCOPE II

K-Number: K926412 · 1994-07-19

ApplicantChiron Vision Corp.
Decision Date1994-07-19
Product CodeHMS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICRON-SCOPE II is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1994-07-19 under 510(k) number K926412. The device is classified under product code HMS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRON-SCOPE II?

MICRON-SCOPE II is a medical device that received FDA 510(k) clearance on 1994-07-19. The listed applicant is Chiron Vision Corp.. The 510(k) number is K926412.

When did MICRON-SCOPE II receive FDA 510(k) clearance?

MICRON-SCOPE II received FDA 510(k) clearance on 1994-07-19, under 510(k) number K926412.

Who is the listed applicant for MICRON-SCOPE II?

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

What is the FDA product code for MICRON-SCOPE II?

The FDA product code for MICRON-SCOPE II is HMS.

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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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