SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE
K-Number: K926495 · 1994-02-02
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Device Summary
Frequently Asked Questions
What is the SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE?
SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE is a medical device that received FDA 510(k) clearance on 1994-02-02. The listed applicant is Sil-Med Corp.. The 510(k) number is K926495.
When did SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE receive FDA 510(k) clearance?
SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE received FDA 510(k) clearance on 1994-02-02, under 510(k) number K926495.
Who is the listed applicant for SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE?
The FDA 510(k) record lists Sil-Med Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE?
The FDA product code for SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE is GBX.
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 Sil-Med Corp. 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: GBX)
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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