ACON DIGITAL THERMOMETER PROBE COVERS
K-Number: K063418 · 2007-02-02
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Device Summary
Frequently Asked Questions
What is the ACON DIGITAL THERMOMETER PROBE COVERS?
ACON DIGITAL THERMOMETER PROBE COVERS is a medical device that received FDA 510(k) clearance on 2007-02-02. The listed applicant is ACON Laboratories, Inc.. The 510(k) number is K063418.
When did ACON DIGITAL THERMOMETER PROBE COVERS receive FDA 510(k) clearance?
ACON DIGITAL THERMOMETER PROBE COVERS received FDA 510(k) clearance on 2007-02-02, under 510(k) number K063418.
Who is the listed applicant for ACON DIGITAL THERMOMETER PROBE COVERS?
The FDA 510(k) record lists ACON Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACON DIGITAL THERMOMETER PROBE COVERS?
The FDA product code for ACON DIGITAL THERMOMETER PROBE COVERS is FLL.
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 ACON Laboratories, 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: FLL)
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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