PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG
K-Number: K841986 · 1984-09-10
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Device Summary
Frequently Asked Questions
What is the PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG?
PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG is a medical device that received FDA 510(k) clearance on 1984-09-10. The listed applicant is Protomed Corp.. The 510(k) number is K841986.
When did PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG receive FDA 510(k) clearance?
PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG received FDA 510(k) clearance on 1984-09-10, under 510(k) number K841986.
Who is the listed applicant for PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG?
The FDA 510(k) record lists Protomed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG?
The FDA product code for PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG is KNT.
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: KNT)
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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