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FDA 510(k)

CONMED VENI-GARD I.V. DRESSING

K-Number: K935389 · 1994-03-07

ApplicantConmedcorp
Decision Date1994-03-07
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONMED VENI-GARD I.V. DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K935389. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED VENI-GARD I.V. DRESSING?

CONMED VENI-GARD I.V. DRESSING is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Conmedcorp. The 510(k) number is K935389.

When did CONMED VENI-GARD I.V. DRESSING receive FDA 510(k) clearance?

CONMED VENI-GARD I.V. DRESSING received FDA 510(k) clearance on 1994-03-07, under 510(k) number K935389.

Who is the listed applicant for CONMED VENI-GARD I.V. DRESSING?

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

What is the FDA product code for CONMED VENI-GARD I.V. DRESSING?

The FDA product code for CONMED VENI-GARD I.V. DRESSING is KMK.

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Other records listing Conmedcorp 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.

K101534CONMED ALTRUS THERMAL TISSUE FUSION SYSTEMK061021ENTAKE STANDARD AND SAFETY PEG SYSTEMK050992CONMED IRRIGATION NOZZLEK050777PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907K050304FX WIRE ADVANCED MEASUREMENT GUIDEWIREK041953VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART

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Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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