ANAESLOCK THREE VAPORIZER INTERLOCK HVA003
K-Number: K843993 · 1984-11-15
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Device Summary
Frequently Asked Questions
What is the ANAESLOCK THREE VAPORIZER INTERLOCK HVA003?
ANAESLOCK THREE VAPORIZER INTERLOCK HVA003 is a medical device that received FDA 510(k) clearance on 1984-11-15. The listed applicant is Southmedic, Inc.. The 510(k) number is K843993.
When did ANAESLOCK THREE VAPORIZER INTERLOCK HVA003 receive FDA 510(k) clearance?
ANAESLOCK THREE VAPORIZER INTERLOCK HVA003 received FDA 510(k) clearance on 1984-11-15, under 510(k) number K843993.
Who is the listed applicant for ANAESLOCK THREE VAPORIZER INTERLOCK HVA003?
The FDA 510(k) record lists Southmedic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANAESLOCK THREE VAPORIZER INTERLOCK HVA003?
The FDA product code for ANAESLOCK THREE VAPORIZER INTERLOCK HVA003 is CAD.
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 Southmedic, 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: CAD)
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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