510(k) · Cleared

Cleared

Transport Media

K781304510(k) TraditionalCleared Aug 14, 197818-day reviewClass I21 CFR 866.2390

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Bd Becton Dickinson Vacutainer Systems Preanalytic · JSN Culture Media, Propagating Transport

Cleared on Aug 14, 1978 after an 18-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided: Aug 14, 1978
Review: 18 days
Class: Class I
Product code: JSN
Recalls: None
Predicates: 0

1 later device descends from it, 1 citing it directly.

This deviceK781304 Transport MediaBd Becton Dickinson Vacutainer Systems Preanalytic · 1978
Descendant · cites it directly · 0 of its ownK070062 Coproset Salmonella and Shigella, Uriset Preservative Tubes and Swab…Diesse Diagnostica Senese S.P.A. · 2007

Most influential descendants

Showing 1 of 1 · See all

K070062Coproset Salmonella and Shigella, Uriset Preservative Tubes and Swab Set General UseDiesse Diagnostica Senese S.P.A. · 2007 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K781304	Transport Media	Bd Becton Dickinson Vacutainer Systems Preanalytic	1978	—
+1	K070062	Coproset Salmonella and Shigella, Uriset Preservative Tubes and Swab Set…	Diesse Diagnostica Senese S.P.A.	2007	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2007	1	0

FIG. 1 — Lineage of K781304, 1978–2007Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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.

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Recall history across each candidate’s familyin the report

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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? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K070062	Coproset Salmonella and Shigella, Uriset Preservative Tubes and Swab Set General Use	Diesse Diagnostica Senese S.P.A.	2007	0

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, K070062 (Diesse Diagnostica Senese S.P.A., 2007) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JSN devices

JSN Culture Media, Propagating Transport: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JSN

FDA has decided no JSN device since 2007.

Median 510(k) review, days · JSN

Too few JSN 510(k)s in any year since 2007 to give a median.

Recalls per year · JSN

No recall names JSN since 2007.

Adverse event reports per year · JSN

No MAUDE report names JSN since 2007.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	0
2012	—	0
2013	—	0
2014	—	0
2015	—	0
2016	—	0
2017	—	0
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

https://510kreport.com/device/K781304 · printed Nov 6, 2026

Cite this page

510(k) Report. “K781304: Transport Media.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K781304

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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