SERACON TM SR III
K-Number: K844027 · 1984-11-27
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Device Summary
Frequently Asked Questions
What is the SERACON TM SR III?
SERACON TM SR III is a medical device that received FDA 510(k) clearance on 1984-11-27. The listed applicant is Bhp Diagnostix, Inc.. The 510(k) number is K844027.
When did SERACON TM SR III receive FDA 510(k) clearance?
SERACON TM SR III received FDA 510(k) clearance on 1984-11-27, under 510(k) number K844027.
Who is the listed applicant for SERACON TM SR III?
The FDA 510(k) record lists Bhp Diagnostix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SERACON TM SR III?
The FDA product code for SERACON TM SR III is JIX.
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 Bhp Diagnostix, 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: JIX)
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.
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