OPERAID SURGICAL DRAIN
K-Number: K841721 · 1984-11-21
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Device Summary
Frequently Asked Questions
What is the OPERAID SURGICAL DRAIN?
OPERAID SURGICAL DRAIN is a medical device that received FDA 510(k) clearance on 1984-11-21. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K841721.
When did OPERAID SURGICAL DRAIN receive FDA 510(k) clearance?
OPERAID SURGICAL DRAIN received FDA 510(k) clearance on 1984-11-21, under 510(k) number K841721.
Who is the listed applicant for OPERAID SURGICAL DRAIN?
The FDA 510(k) record lists Jedmed Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPERAID SURGICAL DRAIN?
The FDA product code for OPERAID SURGICAL DRAIN is HOZ.
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 Jedmed Instrument Co. 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: HOZ)
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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