FDA 510(k) Premarket Notification K955248: U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT

Submission Details & Decision

Normalized public record details for 510(k) notification K955248.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K955248

Applicant / Sponsor

United States Endoscopy Group, Inc.

Device Name

U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT

Product Code

KNT

Decision Date

1996-05-21

Decision / Status

Unknown (SESK)

Advisory Committee

Gastroenterology, Urology (GU)

Clearance Type

Traditional

Third Party Flag

Date Received

1995-11-15

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