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FDA 510(k)

CALCIUM

K-Number: K850281 · 1985-02-06

Decision Date1985-02-06
Product CodeCIC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CALCIUM is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1985-02-06 under 510(k) number K850281. The device is classified under product code CIC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALCIUM?

CALCIUM is a medical device that received FDA 510(k) clearance on 1985-02-06. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K850281.

When did CALCIUM receive FDA 510(k) clearance?

CALCIUM received FDA 510(k) clearance on 1985-02-06, under 510(k) number K850281.

Who is the listed applicant for CALCIUM?

The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CALCIUM?

The FDA product code for CALCIUM is CIC.

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.

Related PubMed Literature

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Other records listing Boehringer Mannheim Corp. 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.

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Related Devices (Code: CIC)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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