510(k) Report

510(k) · Cleared

Cleared

Static and Dynamic Compliance, a Respiratory Mechanics Option for the Vmax Series

K981366510(k) TraditionalCleared Oct 30, 1998198-day reviewClass II21 CFR 868.1890

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

Sensor Medics Corp. · BTY Calculator, Predicted Values, Pulmonary Function

Cleared on Oct 30, 1998 after a 198-day review. The FDA summary names its predicate without a number.

Decided
Oct 30, 1998
Review
198 days
Class
Class II
Product code
BTY
Recalls
None
Predicates
0

The FDA summary names its predicate without a number.

FIG. 1 — Lineage of K981366Source: FDA 510(k) database · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 BTY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new BTY device

  1. #1 K260242 CPETWise Platformscore 13.1 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (2)

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.

TypeNumberDeviceApplicantDecidedRecalls
*—SensorMedics Vmax 2900
Named without a submission number
—
*—SensorMedics Vmax 2200
Named without a submission number
—

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.

How does its category compare?

All BTY devices

BTY Calculator, Predicted Values, Pulmonary Function: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · BTY

3in 2024

2007: 22008: 32009: 12010: 12011: 12012: 32016: 12017: 12019: 22020: 12021: 12022: 12023: 12024: 32026 (partial year): 1
2007high 3 (2008) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BTY

266in 2024

2008: 104 days median2012: 139 days median2024: 266 days median
2007high 266 (2024) · low 104 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · BTY

2in 2017

2014: 12017: 2
2007high 2 (2017) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · BTY

5in 2024

2009: 12011: 32012: 22014: 12015: 512016: 242017: 92018: 52019: 32020: 32021: 22022: 22023: 12024: 5
2007high 51 (2015) · low 0 (2007)2025

MAUDE reports naming product code BTY, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—00
2008310400
20091—01
20101—00
20111—03
2012313902
20130—00
20140—11
20150—051
20161—024
20171—29
20180—05
20192—03
20201—03
20211—02
20221—02
20231—01
2024326605
20250—00
20261—0—

What is it indicated for?

The indications for use are the same as the Vmax Series to which this product is an option. Quotation from the Indications for Use section of the Vmax premarket notification: “Basically, this involves performing physician-prescribed pulmonary function and metabolic testing. More-specific intended uses are shown in the table below, along with the predicate SensorMedics product model with the same intended-use labeling.”

The Static and Dynamic Compliance option is indicated specifically for Evaluation of medication effects, Pulmonary Function testing in adults & children, Pulmonary disability evaluation, Industrial surveillance and Bedside lung function.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K981366: Static and Dynamic Compliance, a Respiratory Mechanics Option for the Vmax Series.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K981366

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026