Cleared Traditional

K822712 - INPERSOL-CAPD ADMINIS. SET TYPE DP

K822712 is an FDA 510(k) clearance for INPERSOL-CAPD ADMINIS. SET TYPE DP, manufactured by Abbott Laboratories. The device is a Class 2 Gastroenterology & Urology device with product code FKX cleared through the Traditional 510(k) pathway after a 44-day FDA review.

K822712 · Abbott Laboratories · Gastroenterology & Urology device
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Oct 1982
Decision
44d
Days
Class 2
Risk

K822712 is an FDA 510(k) clearance for the INPERSOL-CAPD ADMINIS. SET TYPE DP. Classified as System, Peritoneal, Automatic Delivery (product code FKX), Class II - Special Controls.

Submitted by Abbott Laboratories (Abbott Park, US). The FDA issued a Cleared decision on October 21, 1982 after a review of 44 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5630 - the FDA gastroenterology and urology 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Abbott Laboratories devices

FDA 510(k) Submission Details - K822712

510(k) Number K822712 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 07, 1982
Decision Date October 21, 1982
Days to Decision 44 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
86d faster than avg
Panel avg: 130d · This submission: 44d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FKX Device Classification - Class 2, Special Controls

Product Code FKX System, Peritoneal, Automatic Delivery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5630
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FKX System, Peritoneal, Automatic Delivery

All 60
Devices cleared under the same product code (FKX) and FDA review panel - the closest regulatory comparables to K822712.
STERILE, DISPOS. SPIKE PROTECTOR-5C4138
K823777 · Travenol Laboratories, S.A. · Jan 1983
INPERSOL PERITONEAL DIALSIS CYCLER SET
K823217 · Abbott Laboratories · Nov 1982
EXTENSION SET TYPE DP
K822658 · Abbott Laboratories · Oct 1982
CAPD SAFE LOCK TRANSFER SET
K822543 · American Medical Products, Inc. · Oct 1982
SAFE LOCK SEALING CAP L
K822544 · American Medical Products, Inc. · Oct 1982
CCPD CYCLER SET W/5 PRONGED CONNECTOR
K822545 · American Medical Products, Inc. · Oct 1982