Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Med-Tainer Single Deposit Container

K-Number: K153274 · 2016-08-04

Decision Date2016-08-04
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Med-Tainer Single Deposit Container is the device name listed in this FDA 510(k) record. The listed applicant is Snyder Industries, Inc.. It received FDA 510(k) clearance on 2016-08-04 under 510(k) number K153274. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Med-Tainer Single Deposit Container?

Med-Tainer Single Deposit Container is a medical device that received FDA 510(k) clearance on 2016-08-04. The listed applicant is Snyder Industries, Inc.. The 510(k) number is K153274.

When did Med-Tainer Single Deposit Container receive FDA 510(k) clearance?

Med-Tainer Single Deposit Container received FDA 510(k) clearance on 2016-08-04, under 510(k) number K153274.

Who is the listed applicant for Med-Tainer Single Deposit Container?

The FDA 510(k) record lists Snyder Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Med-Tainer Single Deposit Container?

The FDA product code for Med-Tainer Single Deposit Container is MMK.

Related Devices (Code: MMK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.