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FDA 510(k)

BEMIS TWO GALLON SHARPS CONTAINER

K-Number: K965248 · 1997-02-14

ApplicantBemis Mfg. Co.
Decision Date1997-02-14
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BEMIS TWO GALLON SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Bemis Mfg. Co.. It received FDA 510(k) clearance on 1997-02-14 under 510(k) number K965248. 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 BEMIS TWO GALLON SHARPS CONTAINER?

BEMIS TWO GALLON SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 1997-02-14. The listed applicant is Bemis Mfg. Co.. The 510(k) number is K965248.

When did BEMIS TWO GALLON SHARPS CONTAINER receive FDA 510(k) clearance?

BEMIS TWO GALLON SHARPS CONTAINER received FDA 510(k) clearance on 1997-02-14, under 510(k) number K965248.

Who is the listed applicant for BEMIS TWO GALLON SHARPS CONTAINER?

The FDA 510(k) record lists Bemis Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEMIS TWO GALLON SHARPS CONTAINER?

The FDA product code for BEMIS TWO GALLON SHARPS CONTAINER is FMI.

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Other records listing Bemis Mfg. Co. 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.

K020921NO-POKES NEEDLE SAFETY DEVICEK964858BEMIS TWO GALLON CHEMOTHERAPY CONTAINERK960525BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)K953797SHARPS DISPOSAL CONTAINERSK950340IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERSK941664SHARP DISPOSAL CONTAINERS WALL SAFE

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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.

K261266MOWANA™ Auto DuoPENTAMASTER MEDIQ SDN BHDK261719Promisemed X-Safety Pen NeedlePromisemed Hangzhou Meditech Co., Ltd.K262427Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety Type IIIB, Safety Type IV, Safety Type V, Ordinary Type VIA, Ordinary Type VIB, Ordinary Type VIC, Safety Type VII, Ordinary Type IB, Safety type VIII, Safety Type IX, Safety Type X, Ordinary Type XI, Safety Type XII)Hh Global Technology, Inc.K260933Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R, NR-S2016R, NR-S2025R, NR-S2038R, NR-S2051R, NR-S2116R, NR-S2125R, NR-S2138R, NR-S2151R, NR-S2216R, NR-S2225R, NR-S2238R, NR-S2251R, NR-S2316R, NR-S2325R, NR-S2338R, NR-S2351R, NR-S2516R, NR-S2525R, NR-S2538R, NR-S2551R, NR-S2516T, NR-S2525T, NR-S2538T, NR-S2551T)Hangzhou Qiantang Longyue Biotechnology Co., Ltd.K261829Profoject™ Dual-Safety Pen NeedlesCMT Health PTE., Ltd.K260739Profoject™ Pen Needles (Model A; Model B)CMT Health PTE., Ltd.

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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