DERMTRODE
K-Number: K883869 · 1988-09-30
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Device Summary
Frequently Asked Questions
What is the DERMTRODE?
DERMTRODE is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is World Precision Instruments, Inc.. The 510(k) number is K883869.
When did DERMTRODE receive FDA 510(k) clearance?
DERMTRODE received FDA 510(k) clearance on 1988-09-30, under 510(k) number K883869.
Who is the listed applicant for DERMTRODE?
The FDA 510(k) record lists World Precision Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DERMTRODE?
The FDA product code for DERMTRODE is GYA.
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 World Precision Instruments, 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: GYA)
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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