ISOLATION BAG 3M
K-Number: K832318 · 1983-10-31
Advertisement
Device Summary
Frequently Asked Questions
What is the ISOLATION BAG 3M?
ISOLATION BAG 3M is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is 3M Company. The 510(k) number is K832318.
When did ISOLATION BAG 3M receive FDA 510(k) clearance?
ISOLATION BAG 3M received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832318.
Who is the listed applicant for ISOLATION BAG 3M?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ISOLATION BAG 3M?
The FDA product code for ISOLATION BAG 3M is KGY.
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 3M Company 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: KGY)
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