Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIFE PULSE TESUSCITATION TIMER

K-Number: K944667 · 1994-10-04

Decision Date1994-10-04
Product CodePMK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFE PULSE TESUSCITATION TIMER is the device name listed in this FDA 510(k) record. The listed applicant is Green Field Medical Sourcing, Inc.. It received FDA 510(k) clearance on 1994-10-04 under 510(k) number K944667. The device is classified under product code PMK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE PULSE TESUSCITATION TIMER?

LIFE PULSE TESUSCITATION TIMER is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Green Field Medical Sourcing, Inc.. The 510(k) number is K944667.

When did LIFE PULSE TESUSCITATION TIMER receive FDA 510(k) clearance?

LIFE PULSE TESUSCITATION TIMER received FDA 510(k) clearance on 1994-10-04, under 510(k) number K944667.

Who is the listed applicant for LIFE PULSE TESUSCITATION TIMER?

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

What is the FDA product code for LIFE PULSE TESUSCITATION TIMER?

The FDA product code for LIFE PULSE TESUSCITATION TIMER is PMK.

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 Green Field Medical Sourcing, 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.

Related Devices (Code: PMK)

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.

↑