EMMON 3 SABDEX
K-Number: K834322 · 1984-01-13
Advertisement
Device Summary
Frequently Asked Questions
What is the EMMON 3 SABDEX?
EMMON 3 SABDEX is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Hardy Media. The 510(k) number is K834322.
When did EMMON 3 SABDEX receive FDA 510(k) clearance?
EMMON 3 SABDEX received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834322.
Who is the listed applicant for EMMON 3 SABDEX?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMMON 3 SABDEX?
The FDA product code for EMMON 3 SABDEX is JSG.
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 Hardy Media 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: JSG)
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