CONPHAR ARM SLINGS
K-Number: K803139 · 1981-01-08
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Device Summary
Frequently Asked Questions
What is the CONPHAR ARM SLINGS?
CONPHAR ARM SLINGS is a medical device that received FDA 510(k) clearance on 1981-01-08. The listed applicant is Conphar, Inc.. The 510(k) number is K803139.
When did CONPHAR ARM SLINGS receive FDA 510(k) clearance?
CONPHAR ARM SLINGS received FDA 510(k) clearance on 1981-01-08, under 510(k) number K803139.
Who is the listed applicant for CONPHAR ARM SLINGS?
The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONPHAR ARM SLINGS?
The FDA product code for CONPHAR ARM SLINGS is ILI.
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 Conphar, 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: ILI)
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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