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)

ADJUSTABLE FORK RETRACTOR

K-Number: K833604 · 1984-01-03

ApplicantMicrotek Medical, Inc.
Decision Date1984-01-03
Product CodeKAL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ADJUSTABLE FORK RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Microtek Medical, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833604. The device is classified under product code KAL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADJUSTABLE FORK RETRACTOR?

ADJUSTABLE FORK RETRACTOR is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Microtek Medical, Inc.. The 510(k) number is K833604.

When did ADJUSTABLE FORK RETRACTOR receive FDA 510(k) clearance?

ADJUSTABLE FORK RETRACTOR received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833604.

Who is the listed applicant for ADJUSTABLE FORK RETRACTOR?

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

What is the FDA product code for ADJUSTABLE FORK RETRACTOR?

The FDA product code for ADJUSTABLE FORK RETRACTOR is KAL.

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 Microtek Medical, 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.

K110358VENODYNE V810K102971FREEDOMAIRE III SURGICAL HELMET SYSTEM MODEL 10322STKK062899MICROTEK MEDICAL SURGICAL GOWN/TOGAK060200MICROTEK MEDICAL WARMING DRAPEK050322MICROTEK EQUIPMENT DRAPESK022903CHILLBUSTER

View all 24 devices →

Related Devices (Code: KAL)

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.

K870758SMALL MASTOID RETRACTORTreace Medical, Inc.K772381RING HANDLE & RETRACTORSEdward Weck, Inc.K772392ALLPORT MASTOID RETRACTORSEdward Weck, Inc.K760851CONVERSE ALTAR RETRACTORV. Mueller O.V. Baxter Healthcare 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.

↑