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FDA 510(k)

PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY

K-Number: K955790 · 1996-03-21

ApplicantTrylon Corp.
Decision Date1996-03-21
Product CodeHIC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Trylon Corp.. It received FDA 510(k) clearance on 1996-03-21 under 510(k) number K955790. 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 PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY?

PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY is a medical device that received FDA 510(k) clearance on 1996-03-21. The listed applicant is Trylon Corp.. The 510(k) number is K955790.

When did PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY receive FDA 510(k) clearance?

PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY received FDA 510(k) clearance on 1996-03-21, under 510(k) number K955790.

Who is the listed applicant for PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY?

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

What is the FDA product code for PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY?

The FDA product code for PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY 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 Trylon Corp. 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.

K033033VIZILITE-BLUE ORAL EXAM KITK011488SPIRABRUSH CX BIOPSY INSTRUMENTK012070ORALLITE COMPREHENSIVE EXAM TRAYK003995SPECULITE/ORALLITEK963391SPECULITEK953364SPECULITE

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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.

K923656LIGHTING SOURCE SYSTEMGalenica Enterprises, Inc.K902516NEW LENGTH SUGITA APPLIERSSims Surgical, 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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