FDA 510(k)

MEDI-PLAST DISPOSABLE MANIFOLD

K-Number: K863402 · 1986-10-22

Decision Date1986-10-22

Product CodeDTL

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDI-PLAST DISPOSABLE MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Plast Intl., Inc.. It received FDA 510(k) clearance on 1986-10-22 under 510(k) number K863402. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-PLAST DISPOSABLE MANIFOLD?

MEDI-PLAST DISPOSABLE MANIFOLD is a medical device that received FDA 510(k) clearance on 1986-10-22. The listed applicant is Medi-Plast Intl., Inc.. The 510(k) number is K863402.

When did MEDI-PLAST DISPOSABLE MANIFOLD receive FDA 510(k) clearance?

MEDI-PLAST DISPOSABLE MANIFOLD received FDA 510(k) clearance on 1986-10-22, under 510(k) number K863402.

Who is the listed applicant for MEDI-PLAST DISPOSABLE MANIFOLD?

The FDA 510(k) record lists Medi-Plast Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-PLAST DISPOSABLE MANIFOLD?

The FDA product code for MEDI-PLAST DISPOSABLE MANIFOLD is DTL.

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Other records listing Medi-Plast Intl., Inc. as applicant

K954284MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)K87358810CC CONTROL SYRINGE K861785FLUOROSCOPE BAND BAG K851489ARTERIAL-VENOUS COMPRESSION DRESSING K842136STERILE PAN SET K840021OPERATING ROOM TRAY SET

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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.