LS-8 VISICORDER
K-Number: K790825 · 1979-05-31
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Device Summary
Frequently Asked Questions
What is the LS-8 VISICORDER?
LS-8 VISICORDER is a medical device that received FDA 510(k) clearance on 1979-05-31. The listed applicant is Honeywell, Inc.. The 510(k) number is K790825.
When did LS-8 VISICORDER receive FDA 510(k) clearance?
LS-8 VISICORDER received FDA 510(k) clearance on 1979-05-31, under 510(k) number K790825.
Who is the listed applicant for LS-8 VISICORDER?
The FDA 510(k) record lists Honeywell, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LS-8 VISICORDER?
The FDA product code for LS-8 VISICORDER is DSF.
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 Honeywell, 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: DSF)
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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