Cleared Traditional

VARIOUS KITS

K931634 · Polymint Industrial Co. , Ltd. · General & Plastic Surgery
Nov 1993
Decision
243d
Days
Risk

About This 510(k) Submission

K931634 is an FDA 510(k) clearance for the VARIOUS KITS, a First Aid Kit With Drug, submitted by Polymint Industrial Co. , Ltd. (Golden,, US). The FDA issued a Cleared decision on November 30, 1993, 243 days after receiving the submission on April 1, 1993. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K931634 FDA.gov
FDA Decision Cleared SEKD
Date Received April 01, 1993
Decision Date November 30, 1993
Days to Decision 243 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement

Device Classification

Product Code LRR — First Aid Kit With Drug
Device Class
Definition Note: In Addition To Compliance With Our Convenience Kit Guidance, In Regards To Any Drug Products Contained In This Kit Compliance With The Center For Drug Evaluation Is Required As Well. Www.fda.gov/cder/index.html - This Product Code Has Been Established In Accordance With The May 20, 1997, Guidance Entitled, Convenience Kits Interim Regulatory Guidance, Found At Www.fda.gov/cdrh/ode/convkit.html. This Type Of Convenience Kit, As Listed In The Guidance Above, Is Under Enforcement Discretion, And Does Not Require A Premarket Notification (510(k)) To Market If It Meets All Criteria In The Guidance.

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