510(k) · Decided
DecidedDiscography Kit
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
B. Braun of America, Inc. · IZG System, X-Ray, Photofluorographic
Cleared on Oct 7, 1991 after a 244-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 3 later devices descend from it.
- Decided
- Oct 7, 1991
- Review
- 244 days
- Class
- Class II
- Product code
- IZG
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 1 citing it directly.
- This deviceK910503 Discography KitB. Braun of America, Inc. · 1991
- Descendant · cites it directly · 2 of its ownK033739 Physician Industries' Durameter SyringePhysician Industries, Inc. · 2004
- Descendant · 2 generations on · 0 of its ownK102192 Indiscal Digital ManometerBaylis Medical Co., Inc. · 2011
- Descendant · 2 generations on · 0 of its ownK050753 Stryker DiscmonitorStryker Instruments · 2005
Most influential descendants
Showing 3 of 3 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K910503 | Discography Kit | B. Braun of America, Inc. | 1991 | — |
| +1 | K033739 | Physician Industries' Durameter Syringe | Physician Industries, Inc. | 2004 | — |
| +2 | K102192 | Indiscal Digital Manometer | Baylis Medical Co., Inc. | 2011 | — |
| +2 | K050753 | Stryker Discmonitor | Stryker Instruments | 2005 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2011 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in IZG? 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?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K033739 | Physician Industries' Durameter Syringe | 2004 | 2 |
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?
- Of its descendants, K033739 (Physician Industries, Inc., 2004) has gone furthest, with 2 descendants of its own.
How does its category compare?
All IZG devicesIZG System, X-Ray, Photofluorographic: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · IZG
FDA has decided no IZG device since 2007.
Median 510(k) review, days · IZG
Too few IZG 510(k)s in any year since 2007 to give a median.
Recalls per year · IZG
No recall names IZG since 2007.
Adverse event reports per year · IZG
1in 2008
MAUDE reports naming product code IZG, 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 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 1 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K910503 · printed Nov 3, 2026
Cite this page
510(k) Report. “K910503: Discography Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K910503
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026