MONITOR HS8
K-Number: K782044 · 1979-01-10
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Device Summary
Frequently Asked Questions
What is the MONITOR HS8?
MONITOR HS8 is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Scientific & General Pty. , Ltd.. The 510(k) number is K782044.
When did MONITOR HS8 receive FDA 510(k) clearance?
MONITOR HS8 received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782044.
Who is the listed applicant for MONITOR HS8?
The FDA 510(k) record lists Scientific & General Pty. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MONITOR HS8?
The FDA product code for MONITOR HS8 is BZQ.
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 Scientific & General Pty. , Ltd. 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: BZQ)
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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