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Bemis Mfg. Co.

Sheboygan Falls, WI, US

Bemis Mfg. Co. appears in FDA device records in Sheboygan Falls, WI. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
12
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 12 510(k) clearances for Bemis Mfg. Co. between 1985 and 2002. The busiest year on record is 1994, with 3. The most recent is 2002, with 1.

Clearances by year, as a table
510(k) clearance decisions for Bemis Mfg. Co., by decision year
YearClearances
19851
19911
19921
19943
19952
19961
19972
20021
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K020921NO-POKES NEEDLE SAFETY DEVICEFMISubstantially Equivalent
K965248BEMIS TWO GALLON SHARPS CONTAINERFMISubstantially Equivalent
K964858BEMIS TWO GALLON CHEMOTHERAPY CONTAINERMMKSubstantially Equivalent
K960525BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)MMKSubstantially Equivalent
K953797SHARPS DISPOSAL CONTAINERSMMKSubstantially Equivalent
K950340IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERSMMKSubstantially Equivalent
K941665SHARPS DISPOSAL CONTAINER/PHLEBOTOMYMMKSubstantially Equivalent
K941664SHARP DISPOSAL CONTAINERS WALL SAFEMMKSubstantially Equivalent
K931664SHARPS DISPOSABLE CONTAINERSMMKSubstantially Equivalent
K914601SUCTION CONNECTING TUBINGGCXSubstantially Equivalent
K911576CHEMOTHERAPY CONTAINERKPESubstantially Equivalent
K852335STERILIZATION CONTAINERFRGSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain