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)

OPTICAL FORCEPS

K-Number: K990561 · 1999-05-14

ApplicantPilling Weck Surgical
Decision Date1999-05-14
Product CodeJEK
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

OPTICAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Weck Surgical. It received FDA 510(k) clearance on 1999-05-14 under 510(k) number K990561. The device is classified under product code JEK. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTICAL FORCEPS?

OPTICAL FORCEPS is a medical device that received FDA 510(k) clearance on 1999-05-14. The listed applicant is Pilling Weck Surgical. The 510(k) number is K990561.

When did OPTICAL FORCEPS receive FDA 510(k) clearance?

OPTICAL FORCEPS received FDA 510(k) clearance on 1999-05-14, under 510(k) number K990561.

Who is the listed applicant for OPTICAL FORCEPS?

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

What is the FDA product code for OPTICAL FORCEPS?

The FDA product code for OPTICAL FORCEPS is JEK.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pilling Weck Surgical 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.

K992476PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADSK992174PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMPK990935JACKSON ESOPHAGEAL DILATORK982128SHIKANI-FRENCH SPEAKING VALVE

Related Devices (Code: JEK)

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.

K822198MALLEUS NIPPERSKelleher Corp.K822193FORCEPS FOR USE WITH RIGID ENDOSCOPESKelleher Corp.

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.

↑