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FDA 510(k)

COMBINATION NITE DRAINAGE UNIT

K-Number: K872294 · 1987-12-29

ApplicantArnold Technologies
Decision Date1987-12-29
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COMBINATION NITE DRAINAGE UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Arnold Technologies. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K872294. 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 COMBINATION NITE DRAINAGE UNIT?

COMBINATION NITE DRAINAGE UNIT is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Arnold Technologies. The 510(k) number is K872294.

When did COMBINATION NITE DRAINAGE UNIT receive FDA 510(k) clearance?

COMBINATION NITE DRAINAGE UNIT received FDA 510(k) clearance on 1987-12-29, under 510(k) number K872294.

Who is the listed applicant for COMBINATION NITE DRAINAGE UNIT?

The FDA 510(k) record lists Arnold Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMBINATION NITE DRAINAGE UNIT?

The FDA product code for COMBINATION NITE DRAINAGE UNIT 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 Arnold Technologies 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.

K870136PERSONAL PUNCH

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

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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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