MONITOR HS7
K-Number: K782045 · 1979-01-10
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Device Summary
Frequently Asked Questions
What is the MONITOR HS7?
MONITOR HS7 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 K782045.
When did MONITOR HS7 receive FDA 510(k) clearance?
MONITOR HS7 received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782045.
Who is the listed applicant for MONITOR HS7?
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 HS7?
The FDA product code for MONITOR HS7 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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