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FDA 510(k)

CONPHAR 100% SILICONE FOLEY CATH-STER.

K-Number: K792107 · 1979-11-16

ApplicantConphar, Inc.
Decision Date1979-11-16
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONPHAR 100% SILICONE FOLEY CATH-STER. is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K792107. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR 100% SILICONE FOLEY CATH-STER.?

CONPHAR 100% SILICONE FOLEY CATH-STER. is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Conphar, Inc.. The 510(k) number is K792107.

When did CONPHAR 100% SILICONE FOLEY CATH-STER. receive FDA 510(k) clearance?

CONPHAR 100% SILICONE FOLEY CATH-STER. received FDA 510(k) clearance on 1979-11-16, under 510(k) number K792107.

Who is the listed applicant for CONPHAR 100% SILICONE FOLEY CATH-STER.?

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

What is the FDA product code for CONPHAR 100% SILICONE FOLEY CATH-STER.?

The FDA product code for CONPHAR 100% SILICONE FOLEY CATH-STER. is KOD.

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Other records listing Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

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Related Devices (Code: KOD)

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.

K251864Rubber Utility CatheterC.R. Bard, Inc.K220036Wellead Ureteral CatheterWell Lead Medical Co., Ltd.K220730allFlex Ureteral Catheters, Krait Ureteral CathetersAllwin Medical Devices, Inc.K211032Urinary Catheter 12 Fr, Urinary Catheter 16 FrUrogen Pharma, Ltd.K181979Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent CatheterTeleflexmedical, Inc.K180354UroGen Ureteral CatheterUrogen Pharma, Ltd.

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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