FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917
K-Number: K924023 · 1993-04-14
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Device Summary
Frequently Asked Questions
What is the FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917?
FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917 is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Ferno. The 510(k) number is K924023.
When did FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917 receive FDA 510(k) clearance?
FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917 received FDA 510(k) clearance on 1993-04-14, under 510(k) number K924023.
Who is the listed applicant for FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917?
The FDA 510(k) record lists Ferno as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917?
The FDA product code for FERNO ILLE INFERNO MOIST HEAT THERAPY UT, 916/917 is IRQ.
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 Ferno 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: IRQ)
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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