FDA 510(k)

E-Z LOOP

K-Number: K870577 · 1987-04-17

Decision Date1987-04-17

Product CodeEXB

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

E-Z LOOP 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 1987-04-17 under 510(k) number K870577. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-Z LOOP?

E-Z LOOP is a medical device that received FDA 510(k) clearance on 1987-04-17. The listed applicant is John F. Greer Co., Inc.. The 510(k) number is K870577.

When did E-Z LOOP receive FDA 510(k) clearance?

E-Z LOOP received FDA 510(k) clearance on 1987-04-17, under 510(k) number K870577.

Who is the listed applicant for E-Z LOOP?

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 LOOP?

The FDA product code for E-Z LOOP is EXB.

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.

K870531EZ TAC FILTER K864190E-Z HOLD - #4060 K864189ULTRA-GEL - #4083 K864188E-Z HOLD WITH ADHESIVE BASE.-#4065

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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.