SHARPS DISPOSAL CONTAINER/PHLEBOTOMY
K-Number: K941665 · 1994-05-23
Advertisement
Device Summary
Frequently Asked Questions
What is the SHARPS DISPOSAL CONTAINER/PHLEBOTOMY?
SHARPS DISPOSAL CONTAINER/PHLEBOTOMY is a medical device that received FDA 510(k) clearance on 1994-05-23. The listed applicant is Bemis Mfg. Co.. The 510(k) number is K941665.
When did SHARPS DISPOSAL CONTAINER/PHLEBOTOMY receive FDA 510(k) clearance?
SHARPS DISPOSAL CONTAINER/PHLEBOTOMY received FDA 510(k) clearance on 1994-05-23, under 510(k) number K941665.
Who is the listed applicant for SHARPS DISPOSAL CONTAINER/PHLEBOTOMY?
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 SHARPS DISPOSAL CONTAINER/PHLEBOTOMY?
The FDA product code for SHARPS DISPOSAL CONTAINER/PHLEBOTOMY is MMK.
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 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.
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.
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.
Advertisement