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FDA 510(k)

ACKRAD MPR DRAINAGE CATHETER SET

K-Number: K901574 · 1990-06-29

ApplicantAckrad Laboratories
Decision Date1990-06-29
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACKRAD MPR DRAINAGE CATHETER 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 1990-06-29 under 510(k) number K901574. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACKRAD MPR DRAINAGE CATHETER SET?

ACKRAD MPR DRAINAGE CATHETER SET is a medical device that received FDA 510(k) clearance on 1990-06-29. The listed applicant is Ackrad Laboratories. The 510(k) number is K901574.

When did ACKRAD MPR DRAINAGE CATHETER SET receive FDA 510(k) clearance?

ACKRAD MPR DRAINAGE CATHETER SET received FDA 510(k) clearance on 1990-06-29, under 510(k) number K901574.

Who is the listed applicant for ACKRAD MPR DRAINAGE CATHETER 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 MPR DRAINAGE CATHETER SET?

The FDA product code for ACKRAD MPR DRAINAGE CATHETER SET is KNT.

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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: KNT)

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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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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