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FDA 510(k)

VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE

K-Number: K860771 · 1986-04-23

ApplicantVan-Tec, Inc.
Decision Date1986-04-23
Product CodeGCQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1986-04-23 under 510(k) number K860771. The device is classified under product code GCQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE?

VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is Van-Tec, Inc.. The 510(k) number is K860771.

When did VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE receive FDA 510(k) clearance?

VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE received FDA 510(k) clearance on 1986-04-23, under 510(k) number K860771.

Who is the listed applicant for VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE?

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

What is the FDA product code for VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE?

The FDA product code for VAN-TEC DISPOSABLE FLEXIBLE ENDOSCOPE is GCQ.

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Other records listing Van-Tec, 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.

K880099VAN-TEC BLADDER EVACUATORK880095BERGER PROSTATE CULTURE CYTOLOGY BRUSHK880096VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUPK880098VAN-TEC AUTO BIOPSY NEEDLEK880094VAN-TEC ENDOPYELOTOMY KNIFEK874112VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER

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Related Devices (Code: GCQ)

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.

K920979CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340)Codman & Shurtleff, Inc.K900894MEDILASE SERIES 2100 ENDOSCOPEMedical Laser, Inc.K871978CODMAN FLEXIBLE ENDOSCOPECodman & Shurtleff, Inc.K864960TV-ENDOSCOPE, UPPER & LOWER GASTROINTESTINAL APPL.Cooper Lasersonics, 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.

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