Cleared Traditional

K981940 - MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES

K981940 is an FDA 510(k) clearance for MULTAPUMP DISPOSABLE PUMP HEAD AND ACCE..., manufactured by Dexide, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GCJ cleared through the Traditional 510(k) pathway after a 115-day FDA review.

K981940 · Dexide, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1998
Decision
115d
Days
Class 2
Risk

K981940 is an FDA 510(k) clearance for the MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES. Classified as Laparoscope, General & Plastic Surgery (product code GCJ), Class II - Special Controls.

Submitted by Dexide, Inc. (Fort Worth, US). The FDA issued a Cleared decision on September 25, 1998 after a review of 115 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 876.1500 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Dexide, Inc. devices

FDA 510(k) Submission Details - K981940

510(k) Number K981940 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 02, 1998
Decision Date September 25, 1998
Days to Decision 115 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
At panel average
Panel avg: 115d · This submission: 115d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GCJ Device Classification - Class 2, Special Controls

Product Code GCJ Laparoscope, General & Plastic Surgery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition 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).
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GCJ Laparoscope, General & Plastic Surgery

All 1072
Devices cleared under the same product code (GCJ) and FDA review panel - the closest regulatory comparables to K981940.
MGB LAPALUX TELESCOPE
K982013 · Mgb Endoskopische Gerate GmbH · Oct 1998
INNERDYNE STEP TROCAR EXPANDABLE PORT, STEP
K982417 · Innerdyne, Inc. · Oct 1998
AESCULAP NEEDLESCOPIC INSTRUMENT SYSTEM
K982623 · Aesculap, Inc. · Sep 1998
ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM
K982073 · Anchor Products Co. · Sep 1998
MODULAP
K982445 · Atc Medical Technology, Inc. · Sep 1998
ALBATECH PERSONAL MONITOR
K981999 · Albatech, Inc. · Sep 1998