ULTRACELL RETRACTOR COVERS
K-Number: K950659 · 1995-04-13
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Device Summary
Frequently Asked Questions
What is the ULTRACELL RETRACTOR COVERS?
ULTRACELL RETRACTOR COVERS is a medical device that received FDA 510(k) clearance on 1995-04-13. The listed applicant is Ultracell Medical Technologies, Inc.. The 510(k) number is K950659.
When did ULTRACELL RETRACTOR COVERS receive FDA 510(k) clearance?
ULTRACELL RETRACTOR COVERS received FDA 510(k) clearance on 1995-04-13, under 510(k) number K950659.
Who is the listed applicant for ULTRACELL RETRACTOR COVERS?
The FDA 510(k) record lists Ultracell Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRACELL RETRACTOR COVERS?
The FDA product code for ULTRACELL RETRACTOR COVERS is GDY.
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 Ultracell Medical Technologies, 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: GDY)
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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