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FDA 510(k)

CATHETER STRAP & RUINARY BAY HOLDER

K-Number: K780190 · 1978-02-21

ApplicantBaka Manufacturing Co., Inc.
Decision Date1978-02-21
Product CodeFAQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER STRAP & RUINARY BAY HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Baka Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1978-02-21 under 510(k) number K780190. 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 CATHETER STRAP & RUINARY BAY HOLDER?

CATHETER STRAP & RUINARY BAY HOLDER is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Baka Manufacturing Co., Inc.. The 510(k) number is K780190.

When did CATHETER STRAP & RUINARY BAY HOLDER receive FDA 510(k) clearance?

CATHETER STRAP & RUINARY BAY HOLDER received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780190.

Who is the listed applicant for CATHETER STRAP & RUINARY BAY HOLDER?

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

What is the FDA product code for CATHETER STRAP & RUINARY BAY HOLDER?

The FDA product code for CATHETER STRAP & RUINARY BAY HOLDER 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 Baka Manufacturing 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.

K781800GRIP, HOSPITAL UTILITY

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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