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)

IOP ADJUSTABLE STIRRUP

K-Number: K884558 · 1988-11-17

ApplicantMend Technologies, Inc.
Decision Date1988-11-17
Product CodeBWN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IOP ADJUSTABLE STIRRUP is the device name listed in this FDA 510(k) record. The listed applicant is Mend Technologies, Inc.. It received FDA 510(k) clearance on 1988-11-17 under 510(k) number K884558. The device is classified under product code BWN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IOP ADJUSTABLE STIRRUP?

IOP ADJUSTABLE STIRRUP is a medical device that received FDA 510(k) clearance on 1988-11-17. The listed applicant is Mend Technologies, Inc.. The 510(k) number is K884558.

When did IOP ADJUSTABLE STIRRUP receive FDA 510(k) clearance?

IOP ADJUSTABLE STIRRUP received FDA 510(k) clearance on 1988-11-17, under 510(k) number K884558.

Who is the listed applicant for IOP ADJUSTABLE STIRRUP?

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

What is the FDA product code for IOP ADJUSTABLE STIRRUP?

The FDA product code for IOP ADJUSTABLE STIRRUP is BWN.

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 Mend Technologies, 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.

K924094MEND APCK883867CERVICAL BIOPSY INSTRUMENT

Related Devices (Code: BWN)

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.

K942699AIRFRAME SURGICAL DRAPE SUPPORTAlpha Surgical, Inc.K935441INFINITECH BREATH EZInfinitech, Inc.K925005ISI SELF-SUPPORTING ARMInstrumentation Specialties, Inc.K922288HOLDER, PEDIATRIC POSITIONYamashita and Hemsley Business TrustK910783SHAMPAINE MODEL 3800 OR MURANAKA MODEL OR-604MSmith & Nephew Equipment GroupK902865BAUMER SURGICAL TABLESds Dental, Inc.

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.

↑