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FDA 510(k)

BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)

K-Number: K960525 · 1996-03-28

ApplicantBemis Mfg. Co.
Decision Date1996-03-28
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100) 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 1996-03-28 under 510(k) number K960525. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)?

BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100) is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Bemis Mfg. Co.. The 510(k) number is K960525.

When did BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100) receive FDA 510(k) clearance?

BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100) received FDA 510(k) clearance on 1996-03-28, under 510(k) number K960525.

Who is the listed applicant for BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)?

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 ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)?

The FDA product code for BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100) is MMK.

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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 DEVICEK965248BEMIS TWO GALLON SHARPS CONTAINERK964858BEMIS TWO GALLON CHEMOTHERAPY CONTAINERK953797SHARPS DISPOSAL CONTAINERSK950340IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERSK941664SHARP DISPOSAL CONTAINERS WALL SAFE

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Related Devices (Code: MMK)

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

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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