CEDAR(TM) RETRACTOR RING
K-Number: K873691 · 1987-09-28
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Device Summary
Frequently Asked Questions
What is the CEDAR(TM) RETRACTOR RING?
CEDAR(TM) RETRACTOR RING is a medical device that received FDA 510(k) clearance on 1987-09-28. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K873691.
When did CEDAR(TM) RETRACTOR RING receive FDA 510(k) clearance?
CEDAR(TM) RETRACTOR RING received FDA 510(k) clearance on 1987-09-28, under 510(k) number K873691.
Who is the listed applicant for CEDAR(TM) RETRACTOR RING?
The FDA 510(k) record lists Cedar Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CEDAR(TM) RETRACTOR RING?
The FDA product code for CEDAR(TM) RETRACTOR RING is GZT.
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 Cedar Surgical, 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: GZT)
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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