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FDA 510(k)

CALCIUM REAGENT SYS

K-Number: K840214 · 1984-03-19

ApplicantSclavo, Inc.
Decision Date1984-03-19
Product CodeCHZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CALCIUM REAGENT SYS is the device name listed in this FDA 510(k) record. The listed applicant is Sclavo, Inc.. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K840214. The device is classified under product code CHZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALCIUM REAGENT SYS?

CALCIUM REAGENT SYS is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Sclavo, Inc.. The 510(k) number is K840214.

When did CALCIUM REAGENT SYS receive FDA 510(k) clearance?

CALCIUM REAGENT SYS received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840214.

Who is the listed applicant for CALCIUM REAGENT SYS?

The FDA 510(k) record lists Sclavo, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CALCIUM REAGENT SYS?

The FDA product code for CALCIUM REAGENT SYS is CHZ.

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 Sclavo, Inc. 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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Official Source

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