PER-Q-CATH DRESSING CHANGE TRAY
K-Number: K926063 · 1993-06-07
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Device Summary
Frequently Asked Questions
What is the PER-Q-CATH DRESSING CHANGE TRAY?
PER-Q-CATH DRESSING CHANGE TRAY is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Gesco Intl., Inc.. The 510(k) number is K926063.
When did PER-Q-CATH DRESSING CHANGE TRAY receive FDA 510(k) clearance?
PER-Q-CATH DRESSING CHANGE TRAY received FDA 510(k) clearance on 1993-06-07, under 510(k) number K926063.
Who is the listed applicant for PER-Q-CATH DRESSING CHANGE TRAY?
The FDA 510(k) record lists Gesco Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PER-Q-CATH DRESSING CHANGE TRAY?
The FDA product code for PER-Q-CATH DRESSING CHANGE TRAY is MCY.
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 Gesco Intl., 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: MCY)
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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