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FDA 510(k)

QUANTAPHASE B-12-COBALMIN-FOLATE-

K-Number: K833247 · 1983-10-19

ApplicantBio-Rad
Decision Date1983-10-19
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTAPHASE B-12-COBALMIN-FOLATE- is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K833247. 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 QUANTAPHASE B-12-COBALMIN-FOLATE-?

QUANTAPHASE B-12-COBALMIN-FOLATE- is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Bio-Rad. The 510(k) number is K833247.

When did QUANTAPHASE B-12-COBALMIN-FOLATE- receive FDA 510(k) clearance?

QUANTAPHASE B-12-COBALMIN-FOLATE- received FDA 510(k) clearance on 1983-10-19, under 510(k) number K833247.

Who is the listed applicant for QUANTAPHASE B-12-COBALMIN-FOLATE-?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTAPHASE B-12-COBALMIN-FOLATE-?

The FDA product code for QUANTAPHASE B-12-COBALMIN-FOLATE- 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 Bio-Rad 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 319 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.

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