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)

CURVED FINGER SPLINT

K-Number: K820380 · 1982-03-01

Decision Date1982-03-01
Product CodeILH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CURVED FINGER SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Conco Medical Co.. It received FDA 510(k) clearance on 1982-03-01 under 510(k) number K820380. The device is classified under product code ILH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURVED FINGER SPLINT?

CURVED FINGER SPLINT is a medical device that received FDA 510(k) clearance on 1982-03-01. The listed applicant is Conco Medical Co.. The 510(k) number is K820380.

When did CURVED FINGER SPLINT receive FDA 510(k) clearance?

CURVED FINGER SPLINT received FDA 510(k) clearance on 1982-03-01, under 510(k) number K820380.

Who is the listed applicant for CURVED FINGER SPLINT?

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

What is the FDA product code for CURVED FINGER SPLINT?

The FDA product code for CURVED FINGER SPLINT is ILH.

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 Conco Medical Co. 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 12 devices →

Related Devices (Code: ILH)

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.

↑