Tom Cat F.L., Tom Cat S.L.

FDA 510(k) K972245 · A & A Medical, Inc.

Substantially Equivalent

510(k) numberK972245

Submission

Device name
Tom Cat F.L., Tom Cat S.L.
Applicant
A & A Medical, Inc.
Alpharetta, GA, US
Received
June 16, 1997
Decision date
August 6, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MFD – Cannula, Intrauterine Insemination
Device class
Class II (moderate risk)
Regulation
21 CFR 884.5250
Specialty
Obstetrics/Gynecology

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K972823Mini-Embryon Intra Uterine Insemination CatheterMFD · Traditional A & A Medical, Inc.10/10/1997SE
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K963031GenxcatheterMFD · Traditional Genx Intl., Inc.10/21/1996SE

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Questions and answers

When was Tom Cat F.L., Tom Cat S.L. cleared by the FDA?

Tom Cat F.L., Tom Cat S.L. (K972245) received a 510(k) decision of Substantially Equivalent on August 6, 1997, 51 days after the submission was received.

What is the product code of K972245?

The FDA product code is MFD – Cannula, Intrauterine Insemination, a Class II (moderate risk) device regulated under 21 CFR 884.5250.