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FDA 510(k)

MED-SAFE INSULIN SHARPS CONTAINER

K-Number: K943135 · 1994-11-07

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

Device Summary

MED-SAFE INSULIN SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Med-Safe Systems, Inc.. It received FDA 510(k) clearance on 1994-11-07 under 510(k) number K943135. 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 MED-SAFE INSULIN SHARPS CONTAINER?

MED-SAFE INSULIN SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 1994-11-07. The listed applicant is Med-Safe Systems, Inc.. The 510(k) number is K943135.

When did MED-SAFE INSULIN SHARPS CONTAINER receive FDA 510(k) clearance?

MED-SAFE INSULIN SHARPS CONTAINER received FDA 510(k) clearance on 1994-11-07, under 510(k) number K943135.

Who is the listed applicant for MED-SAFE INSULIN SHARPS CONTAINER?

The FDA 510(k) record lists Med-Safe Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED-SAFE INSULIN SHARPS CONTAINER?

The FDA product code for MED-SAFE INSULIN 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 Med-Safe Systems, 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 8 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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