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)

OPTHERM EXTRA FINE TIP

K-Number: K840426 · 1984-05-09

Decision Date1984-05-09
Product CodeHQP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTHERM EXTRA FINE TIP is the device name listed in this FDA 510(k) record. The listed applicant is Suncoast Medical Manufacturers, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K840426. The device is classified under product code HQP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTHERM EXTRA FINE TIP?

OPTHERM EXTRA FINE TIP is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Suncoast Medical Manufacturers, Inc.. The 510(k) number is K840426.

When did OPTHERM EXTRA FINE TIP receive FDA 510(k) clearance?

OPTHERM EXTRA FINE TIP received FDA 510(k) clearance on 1984-05-09, under 510(k) number K840426.

Who is the listed applicant for OPTHERM EXTRA FINE TIP?

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

What is the FDA product code for OPTHERM EXTRA FINE TIP?

The FDA product code for OPTHERM EXTRA FINE TIP is HQP.

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 Suncoast Medical Manufacturers, 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.

View all 31 devices →

Related Devices (Code: HQP)

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.

↑