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FDA 510(k)

NEOPLASTINE CI PLUS

K-Number: K922040 · 1992-06-23

ApplicantAmerican Bioproducts Co.
Decision Date1992-06-23
Product CodeGJS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

NEOPLASTINE CI PLUS is the device name listed in this FDA 510(k) record. The listed applicant is American Bioproducts Co.. It received FDA 510(k) clearance on 1992-06-23 under 510(k) number K922040. The device is classified under product code GJS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOPLASTINE CI PLUS?

NEOPLASTINE CI PLUS is a medical device that received FDA 510(k) clearance on 1992-06-23. The listed applicant is American Bioproducts Co.. The 510(k) number is K922040.

When did NEOPLASTINE CI PLUS receive FDA 510(k) clearance?

NEOPLASTINE CI PLUS received FDA 510(k) clearance on 1992-06-23, under 510(k) number K922040.

Who is the listed applicant for NEOPLASTINE CI PLUS?

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

What is the FDA product code for NEOPLASTINE CI PLUS?

The FDA product code for NEOPLASTINE CI PLUS is GJS.

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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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