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FDA 510(k)

MAS AND MINI-TROL PTH CONTROL

K-Number: K092749 · 2009-12-03

Decision Date2009-12-03
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAS AND MINI-TROL PTH CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Microgenics Corporation. It received FDA 510(k) clearance on 2009-12-03 under 510(k) number K092749. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAS AND MINI-TROL PTH CONTROL?

MAS AND MINI-TROL PTH CONTROL is a medical device that received FDA 510(k) clearance on 2009-12-03. The listed applicant is Microgenics Corporation. The 510(k) number is K092749.

When did MAS AND MINI-TROL PTH CONTROL receive FDA 510(k) clearance?

MAS AND MINI-TROL PTH CONTROL received FDA 510(k) clearance on 2009-12-03, under 510(k) number K092749.

Who is the listed applicant for MAS AND MINI-TROL PTH CONTROL?

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

What is the FDA product code for MAS AND MINI-TROL PTH CONTROL?

The FDA product code for MAS AND MINI-TROL PTH CONTROL is JJX.

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 Microgenics Corporation 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 19 devices →

Related Devices (Code: JJX)

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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