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FDA 510(k)

EZ TAC FILTER

K-Number: K870531 · 1987-04-10

ApplicantJohn F. Greer Co., Inc.
Decision Date1987-04-10
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EZ TAC FILTER 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 1987-04-10 under 510(k) number K870531. 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 EZ TAC FILTER?

EZ TAC FILTER is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is John F. Greer Co., Inc.. The 510(k) number is K870531.

When did EZ TAC FILTER receive FDA 510(k) clearance?

EZ TAC FILTER received FDA 510(k) clearance on 1987-04-10, under 510(k) number K870531.

Who is the listed applicant for EZ TAC FILTER?

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 EZ TAC FILTER?

The FDA product code for EZ TAC FILTER is EXB.

Related Clinical Trials

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.

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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 LOOPK864190E-Z HOLD - #4060K864189ULTRA-GEL - #4083K864188E-Z HOLD WITH ADHESIVE BASE.-#4065

Related Devices (Code: EXB)

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.

K252140Heylo™ SystemColoplast Corp.K181643SmartBag (SmartPouch)11 Health Technologies LimitedK922730LAKE OSTOMY CARE SETLake Medical Products, Inc.K882878ODOR-END EMERGENCY CLEAN UP POWDERCdc Products Corp.K881636CONSEAL COLOSTOMY CONTINENCE SYSTEM (ONE-PIECE)Coloplast A/SK880306EMERGENCY-CLEAN UP(TM) ECPCdc Products Corp.

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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