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FDA 510(k)

DIAL MEDICAL SUPPLY SHARPS CONTAINER

K-Number: K944230 · 1994-11-07

Decision Date1994-11-07
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIAL MEDICAL SUPPLY SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Regulatory & Marketing Services, Inc.. It received FDA 510(k) clearance on 1994-11-07 under 510(k) number K944230. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAL MEDICAL SUPPLY SHARPS CONTAINER?

DIAL MEDICAL SUPPLY SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 1994-11-07. The listed applicant is Regulatory & Marketing Services, Inc.. The 510(k) number is K944230.

When did DIAL MEDICAL SUPPLY SHARPS CONTAINER receive FDA 510(k) clearance?

DIAL MEDICAL SUPPLY SHARPS CONTAINER received FDA 510(k) clearance on 1994-11-07, under 510(k) number K944230.

Who is the listed applicant for DIAL MEDICAL SUPPLY SHARPS CONTAINER?

The FDA 510(k) record lists Regulatory & Marketing Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAL MEDICAL SUPPLY SHARPS CONTAINER?

The FDA product code for DIAL MEDICAL SUPPLY SHARPS CONTAINER is FMI.

Related Clinical Trials

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.

Other records listing Regulatory & Marketing Services, Inc. as applicant

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.

View all 22 devices →

Related Devices (Code: FMI)

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.

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