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FDA 510(k)

ACKRAD H/S PROCEDURE TRAY

K-Number: K881680 · 1988-07-15

ApplicantAckrad Laboratories
Decision Date1988-07-15
Product CodeHIG
Advisory CommitteeOB
DecisionUnknown

Device Summary

ACKRAD H/S PROCEDURE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Ackrad Laboratories. It received FDA 510(k) clearance on 1988-07-15 under 510(k) number K881680. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ACKRAD H/S PROCEDURE TRAY?

ACKRAD H/S PROCEDURE TRAY is a medical device that received FDA 510(k) clearance on 1988-07-15. The listed applicant is Ackrad Laboratories. The 510(k) number is K881680.

When did ACKRAD H/S PROCEDURE TRAY receive FDA 510(k) clearance?

ACKRAD H/S PROCEDURE TRAY received FDA 510(k) clearance on 1988-07-15, under 510(k) number K881680.

Who is the listed applicant for ACKRAD H/S PROCEDURE TRAY?

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 H/S PROCEDURE TRAY?

The FDA product code for ACKRAD H/S PROCEDURE TRAY is HIG.

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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: HIG)

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.

K261706Endomat Select (UP220)KARL STORZ SE & CO. KGK251273Asurys Fluid Management SystemBoston Scientific CorporationK240886Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205)Hologic, Inc.K210628X-FLO Fluid Management SystemThermedx, LLCK201355Endomat Select, IBS Shaver Software, LicenseKarl Storz SE & CO. KGK180735Endomat SelectKarl Storz SE & CO. KG

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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