JUMP START, MODEL 970300
K-Number: K021168 · 2002-06-26
Advertisement
Device Summary
Frequently Asked Questions
What is the JUMP START, MODEL 970300?
JUMP START, MODEL 970300 is a medical device that received FDA 510(k) clearance on 2002-06-26. The listed applicant is Medical Research Laboratories, Inc.. The 510(k) number is K021168.
When did JUMP START, MODEL 970300 receive FDA 510(k) clearance?
JUMP START, MODEL 970300 received FDA 510(k) clearance on 2002-06-26, under 510(k) number K021168.
Who is the listed applicant for JUMP START, MODEL 970300?
The FDA 510(k) record lists Medical Research Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JUMP START, MODEL 970300?
The FDA product code for JUMP START, MODEL 970300 is MKJ. This falls under the Dental category.
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 Medical Research Laboratories, 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: MKJ)
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.
Advertisement