Modular Valve Handles for Adaptable Tubes, Model 1298-XX-XX, 1295-XX-XX

FDA 510(k) K011997 · Pajunk GmbH

Substantially Equivalent

510(k) numberK011997

Submission

Device name
Modular Valve Handles for Adaptable Tubes, Model 1298-XX-XX, 1295-XX-XX
Applicant
Pajunk GmbH
Geisingen, DE
Received
June 27, 2001
Decision date
July 10, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was Modular Valve Handles for Adaptable Tubes, Model 1298-XX-XX, 1295-XX-XX cleared by the FDA?

Modular Valve Handles for Adaptable Tubes, Model 1298-XX-XX, 1295-XX-XX (K011997) received a 510(k) decision of Substantially Equivalent on July 10, 2001, 13 days after the submission was received.

What is the product code of K011997?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.