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FDA 510(k)

BRIO AUTOMATIC SAMPLINC UNIT

K-Number: K961209 · 1996-12-24

ApplicantSeac S.R.L.
Decision Date1996-12-24
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BRIO AUTOMATIC SAMPLINC UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Seac S.R.L.. It received FDA 510(k) clearance on 1996-12-24 under 510(k) number K961209. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRIO AUTOMATIC SAMPLINC UNIT?

BRIO AUTOMATIC SAMPLINC UNIT is a medical device that received FDA 510(k) clearance on 1996-12-24. The listed applicant is Seac S.R.L.. The 510(k) number is K961209.

When did BRIO AUTOMATIC SAMPLINC UNIT receive FDA 510(k) clearance?

BRIO AUTOMATIC SAMPLINC UNIT received FDA 510(k) clearance on 1996-12-24, under 510(k) number K961209.

Who is the listed applicant for BRIO AUTOMATIC SAMPLINC UNIT?

The FDA 510(k) record lists Seac S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRIO AUTOMATIC SAMPLINC UNIT?

The FDA product code for BRIO AUTOMATIC SAMPLINC UNIT is JJF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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