OSMOMETER MODEL 3W11
K-Number: K790611 · 1979-06-15
Advertisement
Device Summary
Frequently Asked Questions
What is the OSMOMETER MODEL 3W11?
OSMOMETER MODEL 3W11 is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Advanced Instruments, Inc.. The 510(k) number is K790611.
When did OSMOMETER MODEL 3W11 receive FDA 510(k) clearance?
OSMOMETER MODEL 3W11 received FDA 510(k) clearance on 1979-06-15, under 510(k) number K790611.
Who is the listed applicant for OSMOMETER MODEL 3W11?
The FDA 510(k) record lists Advanced Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSMOMETER MODEL 3W11?
The FDA product code for OSMOMETER MODEL 3W11 is JJM.
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 Advanced Instruments, Inc. 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: JJM)
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