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FDA 510(k)

ACKRAD RETROGRADE URETHROGRAPHY SET

K-Number: K874312 · 1987-12-29

ApplicantAckrad Laboratories
Decision Date1987-12-29
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACKRAD RETROGRADE URETHROGRAPHY SET is the device name listed in this FDA 510(k) record. The listed applicant is Ackrad Laboratories. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874312. 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 ACKRAD RETROGRADE URETHROGRAPHY SET?

ACKRAD RETROGRADE URETHROGRAPHY SET is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Ackrad Laboratories. The 510(k) number is K874312.

When did ACKRAD RETROGRADE URETHROGRAPHY SET receive FDA 510(k) clearance?

ACKRAD RETROGRADE URETHROGRAPHY SET received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874312.

Who is the listed applicant for ACKRAD RETROGRADE URETHROGRAPHY SET?

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

What is the FDA product code for ACKRAD RETROGRADE URETHROGRAPHY SET?

The FDA product code for ACKRAD RETROGRADE URETHROGRAPHY SET is KOD.

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Other records listing Ackrad Laboratories 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.

K021272SIB CATHETER, MODEL 61-7005K020954H/S PROCEDURE TRAY (5F), H/S PROCEDURE TRAY (7F), H/S ELLIPTOSPHERE PROCEDURE TRAY & MULTIPURPOSE PROCEDURE TRAYK020951H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007K970492INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETERK961752H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)K940176ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION

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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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