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FDA 510(k)

NEW LENGTH SUGITA APPLIERS

K-Number: K902516 · 1990-07-03

ApplicantSims Surgical, Inc.
Decision Date1990-07-03
Product CodeHIC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NEW LENGTH SUGITA APPLIERS is the device name listed in this FDA 510(k) record. The listed applicant is Sims Surgical, Inc.. It received FDA 510(k) clearance on 1990-07-03 under 510(k) number K902516. The device is classified under product code HIC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW LENGTH SUGITA APPLIERS?

NEW LENGTH SUGITA APPLIERS is a medical device that received FDA 510(k) clearance on 1990-07-03. The listed applicant is Sims Surgical, Inc.. The 510(k) number is K902516.

When did NEW LENGTH SUGITA APPLIERS receive FDA 510(k) clearance?

NEW LENGTH SUGITA APPLIERS received FDA 510(k) clearance on 1990-07-03, under 510(k) number K902516.

Who is the listed applicant for NEW LENGTH SUGITA APPLIERS?

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

What is the FDA product code for NEW LENGTH SUGITA APPLIERS?

The FDA product code for NEW LENGTH SUGITA APPLIERS is HIC.

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 Sims Surgical, 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.

K902180TRACHEAL TUBE STYLETK902517NEUROSURGICAL HEADFRAME ACCESSORIES

Related Devices (Code: HIC)

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.

K955790PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAYTrylon Corp.K923656LIGHTING SOURCE SYSTEMGalenica Enterprises, Inc.K897100CENTURION VAGINAL SPECULUMTri-State Hospital Supply Corp.K853257SPECULITE DISPOSABLE VAGINAL LIGHTTrylon Associates, Ltd.

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.

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