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FDA 510(k)

MODIFIED HYSTEROSALPINGOGRAPY SET

K-Number: K871069 · 1987-04-06

ApplicantAckrad Laboratories
Decision Date1987-04-06
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODIFIED HYSTEROSALPINGOGRAPY 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 1987-04-06 under 510(k) number K871069. The device is classified under product code KNA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED HYSTEROSALPINGOGRAPY SET?

MODIFIED HYSTEROSALPINGOGRAPY SET is a medical device that received FDA 510(k) clearance on 1987-04-06. The listed applicant is Ackrad Laboratories. The 510(k) number is K871069.

When did MODIFIED HYSTEROSALPINGOGRAPY SET receive FDA 510(k) clearance?

MODIFIED HYSTEROSALPINGOGRAPY SET received FDA 510(k) clearance on 1987-04-06, under 510(k) number K871069.

Who is the listed applicant for MODIFIED HYSTEROSALPINGOGRAPY 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 MODIFIED HYSTEROSALPINGOGRAPY SET?

The FDA product code for MODIFIED HYSTEROSALPINGOGRAPY SET is KNA.

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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: KNA)

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.

K102141COOK WORD BARTHOLIN GLAND CATHETER (FINAL TRADE NAME NOT YET DETERMINED)Cook Urological, Inc.K093904GLENVEIGH VAGINAL TAMPONADE BALLOON CATHETERGlenveigh Surgical, LLCK082939COOK FETAL MEMBRANE MANIPULATOR, MODEL -FMM-122400Cook Urological, Inc.K062438BAKRI POSTPARTUM BALLOON, MODEL J-SOS-100500Cook Ob/GynK060289EPISTAT, V-STAT, MODELS EPISTAT-001-01, V-STAT-001-01Frontline MedicalK013597TAMPONADE UTERINE BALLOON CATHETER SETCook Ob/Gyn

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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