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)

METRICOM

K-Number: K860225 · 1986-02-11

Decision Date1986-02-11
Product CodeLDK
DecisionSubstantially Equivalent

Device Summary

METRICOM is the device name listed in this FDA 510(k) record. The listed applicant is Far Orthopedics, Inc.. It received FDA 510(k) clearance on 1986-02-11 under 510(k) number K860225. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METRICOM?

METRICOM is a medical device that received FDA 510(k) clearance on 1986-02-11. The listed applicant is Far Orthopedics, Inc.. The 510(k) number is K860225.

When did METRICOM receive FDA 510(k) clearance?

METRICOM received FDA 510(k) clearance on 1986-02-11, under 510(k) number K860225.

Who is the listed applicant for METRICOM?

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

What is the FDA product code for METRICOM?

The FDA product code for METRICOM is LDK.

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 Far Orthopedics, 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: LDK)

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.

↑