Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)

K-Number: K853127 · 1985-09-16

Decision Date1985-09-16
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL) is the device name listed in this FDA 510(k) record. The listed applicant is Micromedic Systems. It received FDA 510(k) clearance on 1985-09-16 under 510(k) number K853127. The device is classified under product code CDD. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 42 devices →

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.

↑