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FDA 510(k)

PER-Q-CATH DRESSING CHANGE TRAY

K-Number: K926063 · 1993-06-07

Decision Date1993-06-07
Product CodeMCY
Advisory CommitteeHO
DecisionUnknown

Device Summary

PER-Q-CATH DRESSING CHANGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Gesco Intl., Inc.. It received FDA 510(k) clearance on 1993-06-07 under 510(k) number K926063. The device is classified under product code MCY. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

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.

View all 26 devices →

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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