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)

REPLICA

K-Number: K925746 · 1994-01-21

ApplicantMatech, Inc.
Decision Date1994-01-21
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REPLICA is the device name listed in this FDA 510(k) record. The listed applicant is Matech, Inc.. It received FDA 510(k) clearance on 1994-01-21 under 510(k) number K925746. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLICA?

REPLICA is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Matech, Inc.. The 510(k) number is K925746.

When did REPLICA receive FDA 510(k) clearance?

REPLICA received FDA 510(k) clearance on 1994-01-21, under 510(k) number K925746.

Who is the listed applicant for REPLICA?

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

What is the FDA product code for REPLICA?

The FDA product code for REPLICA is ELW.

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 Matech, 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: ELW)

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.

↑