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FDA 510(k)

VENTI-GARD JR.

K-Number: K810896 · 1981-04-17

ApplicantCon Med Equipment, Inc.
Decision Date1981-04-17
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENTI-GARD JR. is the device name listed in this FDA 510(k) record. The listed applicant is Con Med Equipment, Inc.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810896. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTI-GARD JR.?

VENTI-GARD JR. is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Con Med Equipment, Inc.. The 510(k) number is K810896.

When did VENTI-GARD JR. receive FDA 510(k) clearance?

VENTI-GARD JR. received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810896.

Who is the listed applicant for VENTI-GARD JR.?

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

What is the FDA product code for VENTI-GARD JR.?

The FDA product code for VENTI-GARD JR. is KGX.

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Other records listing Con Med Equipment, 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.

K830613ELECTROSURGICAL GROUND PAD-DISPERSIVEK810895ESOPHAGEAL PILL ELECTRODE

Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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