PeDIA

FDA 510(k) K181424 · Pedia, LLC

Substantially Equivalent

510(k) numberK181424

Submission

Device name
PeDIA
Applicant
Pedia, LLC
Fairfax, VA, US
Received
May 31, 2018
Decision date
September 25, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTC – Bag, Reservoir
Device class
Class I (low risk)
Regulation
21 CFR 868.5320
Specialty
Anesthesiology

Other 510(k)s with product code BTC

510(k)DeviceApplicantDecision
K940220Rebreather BagsBTC · Traditional Zefon Medical Products05/27/1994SE
K932584Breathing BagsBTC · Traditional Merit Medical Systems, Inc.07/16/1993SE
K932581Breathing BagsBTC · Traditional Med-Plastics Intl., Inc.07/16/1993SE
K932496Precision Med Products, Ltd. Breathing BagsBTC · Traditional Precision Med Products, Ltd.07/16/1993SE
K932191Breathing BagsBTC · Traditional Life Shield Healthcare Products, Inc.07/02/1993SE
K894906Anesthesia Breathing Bags Sizes 1/2, 1,2,3 LiterBTC · Traditional Med-Tek Corp.09/18/1989SE
K880680King Systems, Breathing BagBTC · Traditional King Systems Corp.03/03/1988SE
K864822Varidyne 550, Models 12E,12M,24E & 24M Suction SysBTC · Traditional Surgidyne, Inc.01/15/1987SE
K841412Rolled Neck W/TapBTC · Traditional Warne Surgical Products, Ltd.04/18/1984SE
K841411Rolled Neck W/PlugBTC · Traditional Warne Surgical Products, Ltd.04/18/1984SE

Questions and answers

When was PeDIA cleared by the FDA?

PeDIA (K181424) received a 510(k) decision of Substantially Equivalent on September 25, 2018, 117 days after the submission was received.

What is the product code of K181424?

The FDA product code is BTC – Bag, Reservoir, a Class I (low risk) device regulated under 21 CFR 868.5320.