CATHETER, BETA-CAP-PERITONEAL
K-Number: K782058 · 1979-02-27
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Device Summary
Frequently Asked Questions
What is the CATHETER, BETA-CAP-PERITONEAL?
CATHETER, BETA-CAP-PERITONEAL is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Dravon Medical, Inc.. The 510(k) number is K782058.
When did CATHETER, BETA-CAP-PERITONEAL receive FDA 510(k) clearance?
CATHETER, BETA-CAP-PERITONEAL received FDA 510(k) clearance on 1979-02-27, under 510(k) number K782058.
Who is the listed applicant for CATHETER, BETA-CAP-PERITONEAL?
The FDA 510(k) record lists Dravon Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHETER, BETA-CAP-PERITONEAL?
The FDA product code for CATHETER, BETA-CAP-PERITONEAL is FJS.
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 Dravon Medical, 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: FJS)
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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