Asap Hysteroscope and Gynecologic Laparoscope (Surgery) 10-00018-00, 10-0019-00, 100020-00, 10-0021-00, 10-0022-00, 10-0

FDA 510(k) K031974 · Asap Endoscopic Products GmbH

Substantially Equivalent

510(k) numberK031974

Submission

Device name
Asap Hysteroscope and Gynecologic Laparoscope (Surgery) 10-00018-00, 10-0019-00, 100020-00, 10-0021-00, 10-0022-00, 10-0
Applicant
Asap Endoscopic Products GmbH
Luebeck, DE
Received
June 26, 2003
Decision date
September 29, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HIH – Hysteroscope (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1690
Specialty
Obstetrics/Gynecology

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K240978SeleneView® Single-Use Digital Hysteroscope (HC29, HC29-G, HC35, HC35-G, HO35, HO35-G…HIH · Traditional MacroLux Medical Technology Co., Ltd.08/16/2024SE
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More from Guangzhou Red Pine Medical Instrument Co., Ltd.

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K121261Asap MuitiscopeHRX · Traditional 01/08/2013SE
K032822Asap Sinuscope 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00…EOB · Traditional 01/08/2004SE
K031972Asap Arthroscope Models; 10-0001-00, 10-0002-00, 10-0003-00, 10-0004-00, 10-0005-00…HRX · Traditional 09/15/2003SE
K031141Asap Cystoscope; Asap Laparoscope; Asap Larygoscope; Asap OesophagoscopeFAJ · Traditional 06/30/2003SE

Questions and answers

When was Asap Hysteroscope and Gynecologic Laparoscope (Surgery) 10-00018-00, 10-0019-00, 100020-00, 10-0021-00, 10-0022-00, 10-0 cleared by the FDA?

Asap Hysteroscope and Gynecologic Laparoscope (Surgery) 10-00018-00, 10-0019-00, 100020-00, 10-0021-00, 10-0022-00, 10-0 (K031974) received a 510(k) decision of Substantially Equivalent on September 29, 2003, 95 days after the submission was received.

What is the product code of K031974?

The FDA product code is HIH – Hysteroscope (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1690.