FDA 510(k)

BIPRO MODEL SDS-CB200

K-Number: K033118 · 2004-06-28

ApplicantMedical Solutions International

Decision Date2004-06-28

Product CodeFIN

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BIPRO MODEL SDS-CB200 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Solutions International. It received FDA 510(k) clearance on 2004-06-28 under 510(k) number K033118. The device is classified under product code FIN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIPRO MODEL SDS-CB200?

BIPRO MODEL SDS-CB200 is a medical device that received FDA 510(k) clearance on 2004-06-28. The listed applicant is Medical Solutions International. The 510(k) number is K033118.

When did BIPRO MODEL SDS-CB200 receive FDA 510(k) clearance?

BIPRO MODEL SDS-CB200 received FDA 510(k) clearance on 2004-06-28, under 510(k) number K033118.

Who is the listed applicant for BIPRO MODEL SDS-CB200?

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

What is the FDA product code for BIPRO MODEL SDS-CB200?

The FDA product code for BIPRO MODEL SDS-CB200 is FIN.

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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.