510(k) · Cleared
ClearedPeDIA
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pedia, LLC · BTC Bag, Reservoir
Cleared on Sep 25, 2018 as substantially equivalent to K880680 (King Systems Corp., 1988) after a 117-day review. Its family tree reaches back 1 generation to 1988.
- Decided
- Sep 25, 2018
- Review
- 117 days
- Class
- Class I
- Product code
- BTC
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K880680 (1988). No later device cites it as a predicate yet.
- Root · 1 generation backK880680 King Systems, Breathing BagKing Systems Corp. · 1988
- This deviceK181424 PeDIAPedia, LLC · 2018
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K880680 | King Systems, Breathing Bag | King Systems Corp. | 1988 | — |
| 0 (this device) | K181424 | PeDIA | Pedia, LLC | 2018 | — |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in BTC? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K880680 | King Systems, Breathing BagSummary page 4…C Regulation: 868.5320 III. PREDICATE DEVICES PeDIA is substantially equivalent to the existing class I King Breathing Bags (predicate device - K880680) by King Systems. The proposed PeDIA device is submitted for premarket notification [510(k) pathway] because the addition… | 1988 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Its one ancestor has no recall.
How does its category compare?
All BTC devicesBTC Bag, Reservoir: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.
FDA decisions per year · BTC
1in 2018
2026 to Oct 25, outlined.
Median 510(k) review, days · BTC
Too few BTC 510(k)s in any year since 2007 to give a median.
Recalls per year · BTC
4in 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · BTC
14in 2025
MAUDE reports naming product code BTC, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 4 | 40 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 47 |
| 2011 | 0 | — | 0 | 2 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 1 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 12 |
| 2018 | 1 | — | 0 | 1 |
| 2019 | 0 | — | 0 | 4 |
| 2020 | 0 | — | 0 | 2 |
| 2021 | 0 | — | 0 | 5 |
| 2022 | 0 | — | 0 | 6 |
| 2023 | 0 | — | 0 | 1 |
| 2024 | 0 | — | 0 | 5 |
| 2025 | 0 | — | 0 | 14 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The pediatric device for induction of anesthesia (PeDIA) is an alternative to a face mask for the inhalation induction of anesthesia, and is intended for the delivery of nitrous and/or anesthetic gases to children age three years and older. It is intended to be used prior to IV insertion, LMA/endotracheal intubation, and/or conversion to a standard mask induction
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K181424 · printed Nov 6, 2026
Cite this page
510(k) Report. “K181424: PeDIA.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K181424
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026