HOMECARE CLINICS INFRAHEAT #230
K-Number: K854151 · 1986-01-30
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Device Summary
Frequently Asked Questions
What is the HOMECARE CLINICS INFRAHEAT #230?
HOMECARE CLINICS INFRAHEAT #230 is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is Nelkin/Piper Intl.. The 510(k) number is K854151.
When did HOMECARE CLINICS INFRAHEAT #230 receive FDA 510(k) clearance?
HOMECARE CLINICS INFRAHEAT #230 received FDA 510(k) clearance on 1986-01-30, under 510(k) number K854151.
Who is the listed applicant for HOMECARE CLINICS INFRAHEAT #230?
The FDA 510(k) record lists Nelkin/Piper Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HOMECARE CLINICS INFRAHEAT #230?
The FDA product code for HOMECARE CLINICS INFRAHEAT #230 is ILY.
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.
Related Devices (Code: ILY)
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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