FDA 510(k)

MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)

K-Number: K954284 · 1996-02-12

Decision Date1996-02-12

Product CodeDTL

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON) 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 1996-02-12 under 510(k) number K954284. 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 2 PORT MANIFOLD (RIGHT ON)?

MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON) is a medical device that received FDA 510(k) clearance on 1996-02-12. The listed applicant is Medi-Plast Intl., Inc.. The 510(k) number is K954284.

When did MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON) receive FDA 510(k) clearance?

MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON) received FDA 510(k) clearance on 1996-02-12, under 510(k) number K954284.

Who is the listed applicant for MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)?

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 2 PORT MANIFOLD (RIGHT ON)?

The FDA product code for MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON) is DTL.

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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.