SERACON-A
K-Number: K782037 · 1979-02-08
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Device Summary
Frequently Asked Questions
What is the SERACON-A?
SERACON-A is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Bhp Diagnostix, Inc.. The 510(k) number is K782037.
When did SERACON-A receive FDA 510(k) clearance?
SERACON-A received FDA 510(k) clearance on 1979-02-08, under 510(k) number K782037.
Who is the listed applicant for SERACON-A?
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-A?
The FDA product code for SERACON-A 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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