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FDA 510(k)

VENI-SHIELD

K-Number: K842999 · 1984-09-24

ApplicantU.S. Mfg. & Management, Inc.
Decision Date1984-09-24
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENI-SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Mfg. & Management, Inc.. It received FDA 510(k) clearance on 1984-09-24 under 510(k) number K842999. 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 VENI-SHIELD?

VENI-SHIELD is a medical device that received FDA 510(k) clearance on 1984-09-24. The listed applicant is U.S. Mfg. & Management, Inc.. The 510(k) number is K842999.

When did VENI-SHIELD receive FDA 510(k) clearance?

VENI-SHIELD received FDA 510(k) clearance on 1984-09-24, under 510(k) number K842999.

Who is the listed applicant for VENI-SHIELD?

The FDA 510(k) record lists U.S. Mfg. & Management, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENI-SHIELD?

The FDA product code for VENI-SHIELD is KMK.

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Other records listing U.S. Mfg. & Management, 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.

K920860CONTROLLED PASSIVE MOTION MACHINEK874436FLUID SAMPLING PACKK862335MODIFIED I.V. START, RE-START, PEDI AND GERI-KITK853242I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI

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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