ROUTINE DRESSING TRAY
K-Number: K902811 · 1990-09-25
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Device Summary
Frequently Asked Questions
What is the ROUTINE DRESSING TRAY?
ROUTINE DRESSING TRAY is a medical device that received FDA 510(k) clearance on 1990-09-25. The listed applicant is Orion Life Systems, Inc.. The 510(k) number is K902811.
When did ROUTINE DRESSING TRAY receive FDA 510(k) clearance?
ROUTINE DRESSING TRAY received FDA 510(k) clearance on 1990-09-25, under 510(k) number K902811.
Who is the listed applicant for ROUTINE DRESSING TRAY?
The FDA 510(k) record lists Orion Life Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROUTINE DRESSING TRAY?
The FDA product code for ROUTINE DRESSING 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 Orion Life Systems, 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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