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FDA 510(k)

URINARY DRAINAGE BAG CADDY

K-Number: K931727 · 1993-07-23

ApplicantNeotech Products, Inc.
Decision Date1993-07-23
Product CodeFAQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINARY DRAINAGE BAG CADDY is the device name listed in this FDA 510(k) record. The listed applicant is Neotech Products, Inc.. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K931727. The device is classified under product code FAQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINARY DRAINAGE BAG CADDY?

URINARY DRAINAGE BAG CADDY is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Neotech Products, Inc.. The 510(k) number is K931727.

When did URINARY DRAINAGE BAG CADDY receive FDA 510(k) clearance?

URINARY DRAINAGE BAG CADDY received FDA 510(k) clearance on 1993-07-23, under 510(k) number K931727.

Who is the listed applicant for URINARY DRAINAGE BAG CADDY?

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

What is the FDA product code for URINARY DRAINAGE BAG CADDY?

The FDA product code for URINARY DRAINAGE BAG CADDY is FAQ.

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 Neotech Products, 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.

K011564NEOLEADK921024URO-TOTE LEG BAGK890425NEOTECH MUCUS TRAP W/CATHETERK882203NEOTECH UNIVERSAL ADAPTERK880487NEOTECH MECONIUM ASPIRATOR (STERILE)

Related Devices (Code: FAQ)

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.

K962604PROSYS CUSTOM FIT LEG BAG WITH PREATTACHED ADJUSTABLE INLET TUBE FOR PATIENT SIZINGConvatec, A Division of E.R. Squibb & SonsK960217CPR URINE BAGCustom Pack ReliabilityK955609CONVEEN URINE BAG - STERILEColoplast Corp.K953767PROSYS BEDSIDE DRAINAGE BAGConvatec, A Division of E.R. Squibb & SonsK953783CONVEEN LEG BAG STRAPColoplast Corp.K951945PROSYS LEG BAGConvatec, A Division of E.R. Squibb & Sons

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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