MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)
K-Number: K853127 · 1985-09-16
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Device Summary
Frequently Asked Questions
What is the MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)?
MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL) is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is Micromedic Systems. The 510(k) number is K853127.
When did MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL) receive FDA 510(k) clearance?
MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL) received FDA 510(k) clearance on 1985-09-16, under 510(k) number K853127.
Who is the listed applicant for MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)?
The FDA 510(k) record lists Micromedic Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)?
The FDA product code for MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL) is CDD.
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 Micromedic Systems 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: CDD)
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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