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FDA 510(k)

MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER

K-Number: K972823 · 1997-10-10

ApplicantA & A Medical, Inc.
Decision Date1997-10-10
Product CodeMFD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is A & A Medical, Inc.. It received FDA 510(k) clearance on 1997-10-10 under 510(k) number K972823. The device is classified under product code MFD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER?

MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER is a medical device that received FDA 510(k) clearance on 1997-10-10. The listed applicant is A & A Medical, Inc.. The 510(k) number is K972823.

When did MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER receive FDA 510(k) clearance?

MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER received FDA 510(k) clearance on 1997-10-10, under 510(k) number K972823.

Who is the listed applicant for MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER?

The FDA 510(k) record lists A & A Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER?

The FDA product code for MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER is MFD.

Related Clinical Trials

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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Other records listing A & A Medical, Inc. 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.

K013437SF SH CATHETER, MODEL R65-945K013491HSG CATHETER SET, 5F MODEL RGS0947, HSG CATHETER SET, 7F, MODEL R65-948K003949TACKER, MODEL R65-933K011512MMODIFICATION TO LAMINARIAK010510BALLOON CANNULA, SHORT, MODEL R65-985; BALLOON CANNULA, LONG, MODEL R65-985-1K010789CANNULA, SURGICAL GENERAL & PLASTIC SURGERY, MODELR65-995, R65-995-1, R65-995-2, R65-997, R65-997-1

View all 23 devices →

Related Devices (Code: MFD)

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.

K021438INSEMINATION CATHETER, MODEL 320301Labotect Labor-Technik GottingenK012935THECURVE, ITEM 507Select Medical Systems, Inc.K984306`THE INSEMINATOR' (PROPOSED)Wallach Surgical Devices, Inc.K982630MEDWORKS VISUALIZATION INSEMINATION CATHETERMedworks Corp.K982628MEDWORKS INSEMINATION CATHETERMedworks Corp.K980061EMBRYON INTRAUTERINE INSEMINATION CATHETER, EMRYON SOFT INTRAUTERINE INSEMINATION CATHETER, STYLET FOR EMBRYON INTRAUTERRocket Medical Plc

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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