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)

PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT

K-Number: K810506 · 1981-04-07

ApplicantPropper Mfg. Co., Inc.
Decision Date1981-04-07
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Propper Mfg. Co., Inc.. It received FDA 510(k) clearance on 1981-04-07 under 510(k) number K810506. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT?

PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT is a medical device that received FDA 510(k) clearance on 1981-04-07. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K810506.

When did PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT receive FDA 510(k) clearance?

PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT received FDA 510(k) clearance on 1981-04-07, under 510(k) number K810506.

Who is the listed applicant for PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT?

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

What is the FDA product code for PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT?

The FDA product code for PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT is OCX.

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 Propper Mfg. Co., 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.

K111453STEAM DOT BLU PROCESS INDICATORK102894CLASSIX CHEMICAL STERILIZATION INDICATORK082620ONCE-A-DAY VERTOS TEST PACKK031152PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)K991618BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATORK991276PASS/FAIL CHALLENGE PACK

View all 25 devices →

Related Devices (Code: OCX)

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.

K251986AUXILIARY WATER TUBE MAJ-855Olympus Medical Systems CorporationK251997Single-Use Biopsy Valve (MAJ-1555)Olympus Medical Systems CorporationK242586ArgoCap (200.52)Ovesco Endoscopy AGK241704Endoscopic Water PumpHangzhou AGS MedTech Co., Ltd.K242357Water Container (MAJ-901); Water Container (MAJ-902)Olympus Medical Systems CorporationK241874Aspiration Catheter (2189)Hobbs Medical, 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.

↑