FDA 510(k)

AMERICAN PHARMASEAL I.V. START KIT

K-Number: K842860 · 1984-08-30

Decision Date1984-08-30

Product Code

DecisionSubstantially Equivalent

Device Summary

AMERICAN PHARMASEAL 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 1984-08-30 under 510(k) number K842860. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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

AMERICAN PHARMASEAL I.V. START KIT is a medical device that received FDA 510(k) clearance on 1984-08-30. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K842860.

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

AMERICAN PHARMASEAL I.V. START KIT received FDA 510(k) clearance on 1984-08-30, under 510(k) number K842860.

Who is the listed applicant for AMERICAN PHARMASEAL 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

K874022PHARMASEAL WOUND IRRIGATION DEVICE K874517PHARMASEAL RUBBER URETHRAL CATHETER K874045PHARMASEAL ENDOSCOPY PREP KIT UPPER AND LOWER K873359AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE K872228PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM K872917JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER

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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.