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FDA 510(k)

QUPID PLUS E.R.

K-Number: K020378 · 2002-06-21

ApplicantStanbio Laboratory
Decision Date2002-06-21
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUPID PLUS E.R. is the device name listed in this FDA 510(k) record. The listed applicant is Stanbio Laboratory. It received FDA 510(k) clearance on 2002-06-21 under 510(k) number K020378. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUPID PLUS E.R.?

QUPID PLUS E.R. is a medical device that received FDA 510(k) clearance on 2002-06-21. The listed applicant is Stanbio Laboratory. The 510(k) number is K020378.

When did QUPID PLUS E.R. receive FDA 510(k) clearance?

QUPID PLUS E.R. received FDA 510(k) clearance on 2002-06-21, under 510(k) number K020378.

Who is the listed applicant for QUPID PLUS E.R.?

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

What is the FDA product code for QUPID PLUS E.R.?

The FDA product code for QUPID PLUS E.R. is JHI.

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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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