FDA 510(k)

AMERICAN PHARMASEAL STERILE I.V. START KIT

K-Number: K850266 · 1985-03-22

Decision Date1985-03-22

Product Code

DecisionSubstantially Equivalent

Device Summary

AMERICAN PHARMASEAL STERILE I.V. START KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1985-03-22 under 510(k) number K850266. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERICAN PHARMASEAL STERILE I.V. START KIT?

AMERICAN PHARMASEAL STERILE I.V. START KIT is a medical device that received FDA 510(k) clearance on 1985-03-22. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K850266.

When did AMERICAN PHARMASEAL STERILE I.V. START KIT receive FDA 510(k) clearance?

AMERICAN PHARMASEAL STERILE I.V. START KIT received FDA 510(k) clearance on 1985-03-22, under 510(k) number K850266.

Who is the listed applicant for AMERICAN PHARMASEAL STERILE I.V. START KIT?

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

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Other records listing American Pharmaseal Div. Ahsc as applicant

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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.