DYNACYT BIOPSY ASPIRATION DEVICE
K-Number: K922919 · 1993-03-31
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Device Summary
Frequently Asked Questions
What is the DYNACYT BIOPSY ASPIRATION DEVICE?
DYNACYT BIOPSY ASPIRATION DEVICE is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Buckman Co., Inc.. The 510(k) number is K922919.
When did DYNACYT BIOPSY ASPIRATION DEVICE receive FDA 510(k) clearance?
DYNACYT BIOPSY ASPIRATION DEVICE received FDA 510(k) clearance on 1993-03-31, under 510(k) number K922919.
Who is the listed applicant for DYNACYT BIOPSY ASPIRATION DEVICE?
The FDA 510(k) record lists Buckman Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNACYT BIOPSY ASPIRATION DEVICE?
The FDA product code for DYNACYT BIOPSY ASPIRATION DEVICE is MJG.
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 Buckman Co., 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: MJG)
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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