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FDA 510(k)

POWRSYRINGE MONITOR

K-Number: K072345 · 2007-09-21

ApplicantPinyons Medical Technology, Inc.
Decision Date2007-09-21
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWRSYRINGE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Pinyons Medical Technology, Inc.. It received FDA 510(k) clearance on 2007-09-21 under 510(k) number K072345. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWRSYRINGE MONITOR?

POWRSYRINGE MONITOR is a medical device that received FDA 510(k) clearance on 2007-09-21. The listed applicant is Pinyons Medical Technology, Inc.. The 510(k) number is K072345.

When did POWRSYRINGE MONITOR receive FDA 510(k) clearance?

POWRSYRINGE MONITOR received FDA 510(k) clearance on 2007-09-21, under 510(k) number K072345.

Who is the listed applicant for POWRSYRINGE MONITOR?

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

What is the FDA product code for POWRSYRINGE MONITOR?

The FDA product code for POWRSYRINGE MONITOR is FMF.

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.

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Other records listing Pinyons Medical Technology, 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.

K072299POWRSYRINGE ASPIRATORK072318POWRSYRINGE INJECTOR

Related Devices (Code: FMF)

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

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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