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)

SPIRAL STONE AND RETRIEVAL BASKETS

K-Number: K820429 · 1982-04-08

ApplicantAmerican Endoscopy, Inc.
Decision Date1982-04-08
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SPIRAL STONE AND RETRIEVAL BASKETS is the device name listed in this FDA 510(k) record. The listed applicant is American Endoscopy, Inc.. It received FDA 510(k) clearance on 1982-04-08 under 510(k) number K820429. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIRAL STONE AND RETRIEVAL BASKETS?

SPIRAL STONE AND RETRIEVAL BASKETS is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is American Endoscopy, Inc.. The 510(k) number is K820429.

When did SPIRAL STONE AND RETRIEVAL BASKETS receive FDA 510(k) clearance?

SPIRAL STONE AND RETRIEVAL BASKETS received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820429.

Who is the listed applicant for SPIRAL STONE AND RETRIEVAL BASKETS?

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

What is the FDA product code for SPIRAL STONE AND RETRIEVAL BASKETS?

The FDA product code for SPIRAL STONE AND RETRIEVAL BASKETS is OCZ.

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 American Endoscopy, 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.

K853274AMERICAN DILATATION SYSTEMK841384PROXIMA 1 PH MONITORK833491ENDO BITE BLOCKK840818BIOPSY FORCEPSK833859TAMPONADE BALLOON CUFFK833492PERCUTANEOUS ENDOSCOPIC GASTROSCOPY

View all 19 devices →

Related Devices (Code: OCZ)

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.

K252800KARL STORZ Endoscopic Accessories for UrologyKarl Storz SE & CO. KGK242923SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip Endoscopic Suture Cutter (SC500230)Envision EndoscopyK191900Single Use Grasping ForcepsZhejiang Chuangxiang Medical Technology Co., Ltd.K152802Grasping ForcepsMicro-Tech (Nanjing) Co., Ltd.K120084ENDOSCOPIC RETRIEVAL DEVICEUnited States Endoscopy Group, Inc.K103688G-PROX EZ ENDOSCOPIC GRASPERUsgi Medical

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.

↑