STERIGAGE MODEL 1243RA, 1243RB, 1243RE
K-Number: K101249 · 2010-09-08
Advertisement
Device Summary
Frequently Asked Questions
What is the STERIGAGE MODEL 1243RA, 1243RB, 1243RE?
STERIGAGE MODEL 1243RA, 1243RB, 1243RE is a medical device that received FDA 510(k) clearance on 2010-09-08. The listed applicant is 3M Company. The 510(k) number is K101249.
When did STERIGAGE MODEL 1243RA, 1243RB, 1243RE receive FDA 510(k) clearance?
STERIGAGE MODEL 1243RA, 1243RB, 1243RE received FDA 510(k) clearance on 2010-09-08, under 510(k) number K101249.
Who is the listed applicant for STERIGAGE MODEL 1243RA, 1243RB, 1243RE?
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 STERIGAGE MODEL 1243RA, 1243RB, 1243RE?
The FDA product code for STERIGAGE MODEL 1243RA, 1243RB, 1243RE is JOJ.
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: JOJ)
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