Cardiovit at-5C

K941462510(k) TraditionalCleared May 19, 1995421-day review

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

Schiller America, Inc. · LOS (no longer in FDA’s product-code list)

Cleared on May 19, 1995 after a 421-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: May 19, 1995
Review: 421 days
Product code: LOS
Recalls: None
Predicates: 0

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

This deviceK941462 Cardiovit at-5CSchiller America, Inc. · 1995
Descendant · cites it directly · 0 of its ownK160667 Anybattery C2 Rechargeable BatteryAnybattery, Inc. · 2017

Most influential descendants

Showing 1 of 1 · See all

K160667Anybattery C2 Rechargeable BatteryAnybattery, Inc. · 2017 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K941462	Cardiovit at-5C	Schiller America, Inc.	1995	—
+1	K160667	Anybattery C2 Rechargeable Battery	Anybattery, Inc.	2017	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2017	1	0

FIG. 1 — Lineage of K941462, 1995–2017Source: 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.

Planning a device in LOS? 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

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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
K160667	Anybattery C2 Rechargeable Battery	Anybattery, Inc.	2017	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, K160667 (Anybattery, Inc., 2017) has gone furthest, with 0 descendants of its own.

https://510kreport.com/device/K941462 · printed Nov 6, 2026

Cite this page

510(k) Report. “K941462: Cardiovit at-5C.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K941462

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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