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FDA 510(k)

E-Z HOLD - #4060

K-Number: K864190 · 1987-01-14

ApplicantJohn F. Greer Co., Inc.
Decision Date1987-01-14
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

E-Z HOLD - #4060 is the device name listed in this FDA 510(k) record. The listed applicant is John F. Greer Co., Inc.. It received FDA 510(k) clearance on 1987-01-14 under 510(k) number K864190. 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 E-Z HOLD - #4060?

E-Z HOLD - #4060 is a medical device that received FDA 510(k) clearance on 1987-01-14. The listed applicant is John F. Greer Co., Inc.. The 510(k) number is K864190.

When did E-Z HOLD - #4060 receive FDA 510(k) clearance?

E-Z HOLD - #4060 received FDA 510(k) clearance on 1987-01-14, under 510(k) number K864190.

Who is the listed applicant for E-Z HOLD - #4060?

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

What is the FDA product code for E-Z HOLD - #4060?

The FDA product code for E-Z HOLD - #4060 is KMK.

Other records listing John F. Greer Co., 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.

K870577E-Z LOOPK870531EZ TAC FILTERK864189ULTRA-GEL - #4083K864188E-Z HOLD WITH ADHESIVE BASE.-#4065

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

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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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