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)

MEDCOMP REPAIR KIT, MODEL ASPCRPK

K-Number: K022570 · 2002-10-31

ApplicantMedcomp
Decision Date2002-10-31
Product CodeNFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDCOMP REPAIR KIT, MODEL ASPCRPK is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp. It received FDA 510(k) clearance on 2002-10-31 under 510(k) number K022570. The device is classified under product code NFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCOMP REPAIR KIT, MODEL ASPCRPK?

MEDCOMP REPAIR KIT, MODEL ASPCRPK is a medical device that received FDA 510(k) clearance on 2002-10-31. The listed applicant is Medcomp. The 510(k) number is K022570.

When did MEDCOMP REPAIR KIT, MODEL ASPCRPK receive FDA 510(k) clearance?

MEDCOMP REPAIR KIT, MODEL ASPCRPK received FDA 510(k) clearance on 2002-10-31, under 510(k) number K022570.

Who is the listed applicant for MEDCOMP REPAIR KIT, MODEL ASPCRPK?

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

What is the FDA product code for MEDCOMP REPAIR KIT, MODEL ASPCRPK?

The FDA product code for MEDCOMP REPAIR KIT, MODEL ASPCRPK is NFK.

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 Medcomp 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 39 devices →

Related Devices (Code: NFK)

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.

↑