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FDA 510(k)

ACKRAD FLUID CONNECTING SET

K-Number: K820937 · 1982-04-26

ApplicantAckrad Laboratories
Decision Date1982-04-26
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACKRAD FLUID CONNECTING 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 1982-04-26 under 510(k) number K820937. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACKRAD FLUID CONNECTING SET?

ACKRAD FLUID CONNECTING SET is a medical device that received FDA 510(k) clearance on 1982-04-26. The listed applicant is Ackrad Laboratories. The 510(k) number is K820937.

When did ACKRAD FLUID CONNECTING SET receive FDA 510(k) clearance?

ACKRAD FLUID CONNECTING SET received FDA 510(k) clearance on 1982-04-26, under 510(k) number K820937.

Who is the listed applicant for ACKRAD FLUID CONNECTING 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 FLUID CONNECTING SET?

The FDA product code for ACKRAD FLUID CONNECTING SET is LHI.

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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: LHI)

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.

K252987ADRx™ Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LPK251715FlowArt® Vial Access Device VentedAsset MedikalK251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLCK243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

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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