BIOPSY MEDIUM, MODEL REF 1062
K-Number: K060983 · 2006-07-28
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Device Summary
Frequently Asked Questions
What is the BIOPSY MEDIUM, MODEL REF 1062?
BIOPSY MEDIUM, MODEL REF 1062 is a medical device that received FDA 510(k) clearance on 2006-07-28. The listed applicant is Medicult A/S. The 510(k) number is K060983.
When did BIOPSY MEDIUM, MODEL REF 1062 receive FDA 510(k) clearance?
BIOPSY MEDIUM, MODEL REF 1062 received FDA 510(k) clearance on 2006-07-28, under 510(k) number K060983.
Who is the listed applicant for BIOPSY MEDIUM, MODEL REF 1062?
The FDA 510(k) record lists Medicult A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOPSY MEDIUM, MODEL REF 1062?
The FDA product code for BIOPSY MEDIUM, MODEL REF 1062 is MQL.
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 Medicult A/S 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: MQL)
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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