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FDA 510(k)

SEXTON CYSTOTOMY URINE PUMP (SCUP2)

K-Number: K904434 · 1991-02-01

ApplicantPhoenix Bioengineering, Inc.
Decision Date1991-02-01
Product CodeKOB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SEXTON CYSTOTOMY URINE PUMP (SCUP2) is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Bioengineering, Inc.. It received FDA 510(k) clearance on 1991-02-01 under 510(k) number K904434. The device is classified under product code KOB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEXTON CYSTOTOMY URINE PUMP (SCUP2)?

SEXTON CYSTOTOMY URINE PUMP (SCUP2) is a medical device that received FDA 510(k) clearance on 1991-02-01. The listed applicant is Phoenix Bioengineering, Inc.. The 510(k) number is K904434.

When did SEXTON CYSTOTOMY URINE PUMP (SCUP2) receive FDA 510(k) clearance?

SEXTON CYSTOTOMY URINE PUMP (SCUP2) received FDA 510(k) clearance on 1991-02-01, under 510(k) number K904434.

Who is the listed applicant for SEXTON CYSTOTOMY URINE PUMP (SCUP2)?

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

What is the FDA product code for SEXTON CYSTOTOMY URINE PUMP (SCUP2)?

The FDA product code for SEXTON CYSTOTOMY URINE PUMP (SCUP2) is KOB.

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 Phoenix Bioengineering, 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.

K930125PHOENIX BONE SCREWS PBS-TYPE SERIESK913490PHOENIX BURR HOLE BUTTON, BURR 1

Related Devices (Code: KOB)

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.

K240514AMT Low-Profile Suprapubic Catheter & Drainage SetApplied Medical Technology, Inc.K181097Cook Cystostomy Catheter SetCook IncorporatedK182709One-Step Suprapubic IntroducerCook IncorporatedK182066O'Brien Suprapubic Introducer Set, Cook SP Tube Introducer SetCook IncorporatedK120127SWAN VALLEY MEDICAL TRANURETHRAL SUPRAPUBIC ENDO-CYSTOSTOMY (T-SPEC) SURGICAL SYSTEMSwan Valley Medical, IncorporatedK014002ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890Fortune Medical Instrument 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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