HYSTERECTOMY T DRAIN
K-Number: K782027 · 1978-12-20
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Device Summary
Frequently Asked Questions
What is the HYSTERECTOMY T DRAIN?
HYSTERECTOMY T DRAIN is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Davol, Inc.. The 510(k) number is K782027.
When did HYSTERECTOMY T DRAIN receive FDA 510(k) clearance?
HYSTERECTOMY T DRAIN received FDA 510(k) clearance on 1978-12-20, under 510(k) number K782027.
Who is the listed applicant for HYSTERECTOMY T DRAIN?
The FDA 510(k) record lists Davol, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYSTERECTOMY T DRAIN?
The FDA product code for HYSTERECTOMY T DRAIN is JOL.
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 Davol, 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: JOL)
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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