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FDA 510(k)

LIFE LATCH SHARPS & BIOHAZARD CONTAINER

K-Number: K071088 · 2007-07-05

ApplicantM&M Industries, Inc.
Decision Date2007-07-05
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFE LATCH SHARPS & BIOHAZARD CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is M&M Industries, Inc.. It received FDA 510(k) clearance on 2007-07-05 under 510(k) number K071088. 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 LIFE LATCH SHARPS & BIOHAZARD CONTAINER?

LIFE LATCH SHARPS & BIOHAZARD CONTAINER is a medical device that received FDA 510(k) clearance on 2007-07-05. The listed applicant is M&M Industries, Inc.. The 510(k) number is K071088.

When did LIFE LATCH SHARPS & BIOHAZARD CONTAINER receive FDA 510(k) clearance?

LIFE LATCH SHARPS & BIOHAZARD CONTAINER received FDA 510(k) clearance on 2007-07-05, under 510(k) number K071088.

Who is the listed applicant for LIFE LATCH SHARPS & BIOHAZARD CONTAINER?

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

What is the FDA product code for LIFE LATCH SHARPS & BIOHAZARD CONTAINER?

The FDA product code for LIFE LATCH SHARPS & BIOHAZARD CONTAINER is FMI.

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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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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