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FDA 510(k)

VENSHIELD

K-Number: K941813 · 1994-05-03

ApplicantCybermedic, Inc.
Decision Date1994-05-03
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENSHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Cybermedic, Inc.. It received FDA 510(k) clearance on 1994-05-03 under 510(k) number K941813. The device is classified under product code BYD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENSHIELD?

VENSHIELD is a medical device that received FDA 510(k) clearance on 1994-05-03. The listed applicant is Cybermedic, Inc.. The 510(k) number is K941813.

When did VENSHIELD receive FDA 510(k) clearance?

VENSHIELD received FDA 510(k) clearance on 1994-05-03, under 510(k) number K941813.

Who is the listed applicant for VENSHIELD?

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

What is the FDA product code for VENSHIELD?

The FDA product code for VENSHIELD is BYD.

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Other records listing Cybermedic, 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.

K914205PFF-1K903959NEONATAL METASCOPEK884910MODEL 1010, CY-METK861418SPINNAKERK851197CYBERMEDIC CM-810 BODY PLETHYSMOGRAPHK842782PHYSIOLOGICAL ANALYZER CM-710

View all 11 devices →

Related Devices (Code: BYD)

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.

K955008HEAT & MOISTURE EXCHANGERIntertech Resources, Inc.K954194DISPOSABLE HME/FILTEREngstrom MedicalK953580HEAT MOISTURE EXCHANGERIntertech Resources, Inc.K953507TYPE 1 & 2 (HUMIDAIR I & II)Icor ABK953544HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHTGibeck, Inc.K953620WARM N WET HMEF W/LUER ADAPTERHospitak, 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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