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FDA 510(k)

I.V. TAPE DOWN HOLDER

K-Number: K800024 · 1980-01-29

ApplicantConsolidated Medical Equipment, Inc.
Decision Date1980-01-29
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. TAPE DOWN HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Medical Equipment, Inc.. It received FDA 510(k) clearance on 1980-01-29 under 510(k) number K800024. 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 I.V. TAPE DOWN HOLDER?

I.V. TAPE DOWN HOLDER is a medical device that received FDA 510(k) clearance on 1980-01-29. The listed applicant is Consolidated Medical Equipment, Inc.. The 510(k) number is K800024.

When did I.V. TAPE DOWN HOLDER receive FDA 510(k) clearance?

I.V. TAPE DOWN HOLDER received FDA 510(k) clearance on 1980-01-29, under 510(k) number K800024.

Who is the listed applicant for I.V. TAPE DOWN HOLDER?

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

What is the FDA product code for I.V. TAPE DOWN HOLDER?

The FDA product code for I.V. TAPE DOWN HOLDER is KMK.

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Other records listing Consolidated Medical 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.

K854040I.V. DRESSINGK850130PRN ECG ELECTRODEK850132DISPOSABLE CONDUCTIVE ADHESIVE DIAGNOSTIC ECG ELECK850037CLOSED WOUND DRAINK844942PLURA-GARD CHEST DRAINAGE SYSTEMK850131CONDUCTIVE ADHESIVE POST-OP ELECTRODE-TENS

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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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