ACECUT SUTOMATIC BIOPSY SYSTEM
K-Number: K930201 · 1993-06-09
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Device Summary
Frequently Asked Questions
What is the ACECUT SUTOMATIC BIOPSY SYSTEM?
ACECUT SUTOMATIC BIOPSY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-06-09. The listed applicant is Meadox Surgimed, Inc.. The 510(k) number is K930201.
When did ACECUT SUTOMATIC BIOPSY SYSTEM receive FDA 510(k) clearance?
ACECUT SUTOMATIC BIOPSY SYSTEM received FDA 510(k) clearance on 1993-06-09, under 510(k) number K930201.
Who is the listed applicant for ACECUT SUTOMATIC BIOPSY SYSTEM?
The FDA 510(k) record lists Meadox Surgimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACECUT SUTOMATIC BIOPSY SYSTEM?
The FDA product code for ACECUT SUTOMATIC BIOPSY SYSTEM is KNW.
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 Meadox Surgimed, 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: KNW)
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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