510(k) Report

510(k) · Cleared

Cleared

Utah Disposable Pressure Transducer

K841788510(k) TraditionalCleared Mar 25, 1985329-day reviewClass II21 CFR 870.2850

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

Utah Medical Products, Inc. · DRS Transducer, Blood-Pressure, Extravascular

Cleared on Mar 25, 1985 after a 329-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 7 later devices descend from it.

Decided
Mar 25, 1985
Review
329 days
Class
Class II
Product code
DRS
Recalls
None
Predicates
0

7 later devices descend from it, 4 citing it directly.

Descendants, by year cleared 2007: 1 descendant cleared2010: 1 descendant cleared1998: 1 descendant cleared2000: 1 descendant cleared2015: 1 descendant cleared2011: 1 descendant cleared2002: 1 descendant cleared1990200020102020
  1. This deviceK841788 Utah Disposable Pressure TransducerUtah Medical Products, Inc. · 1985
  2. Descendant · cites it directly · 2 of its ownK070710 Accutrans Disposable Pressure Monitoring SystemBiosensors International-USA · 2007
  3. Descendant · cites it directly · 1 of its ownK991886 Pulsion Pulsiocath, Pulsion Pcco Monitoring Kit, Pulsion in-Line…Pulsion Medical Systems, Inc. · 2000 · Recalled
  4. Descendant · 2 generations on · 0 of its ownK151040 Art-line Single channel blood pressure system, Art-line Double…Biometrix, Ltd. · 2015
  5. Descendant · 2 generations on · 0 of its ownK102033 Combitrans Monitoring Sets and AccessoriesB.Braun Melsungen AG · 2011
  6. Descendant · cites it directly · 0 of its ownK101189 Reavillmed Pressure Monitoring System and PiccReavillmed · 2010

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

1998: 12000: 12002: 12007: 12010: 12011: 12015: 1
1998high 1 (1998) · low 0 (1999)2026

Most influential descendants

Showing 5 of 7 · See all
  • K070710Accutrans Disposable Pressure Monitoring SystemBiosensors International-USA · 2007 · cites it directly2descendants
  • K991886Pulsion Pulsiocath, Pulsion Pcco Monitoring Kit, Pulsion in-Line Injectate SensorPulsion Medical Systems, Inc. · 2000 · cites it directly1descendant
  • K151040Art-line Single channel blood pressure system, Art-line Double channel blood pressure…Biometrix, Ltd. · 2015 · 2 generations on0descendants
  • K102033Combitrans Monitoring Sets and AccessoriesB.Braun Melsungen AG · 2011 · 2 generations on0descendants
  • K101189Reavillmed Pressure Monitoring System and PiccReavillmed · 2010 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K841788Utah Disposable Pressure TransducerUtah Medical Products, Inc.1985—
+1K070710Accutrans Disposable Pressure Monitoring SystemBiosensors International-USA2007—
+1K991886Pulsion Pulsiocath, Pulsion Pcco Monitoring Kit, Pulsion in-Line Injectate…Pulsion Medical Systems, Inc.20001
+2K151040Art-line Single channel blood pressure system, Art-line Double channel blood…Biometrix, Ltd.2015—
+2K102033Combitrans Monitoring Sets and AccessoriesB.Braun Melsungen AG2011—
+1K101189Reavillmed Pressure Monitoring System and PiccReavillmed2010—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
200010
200210
200710
201010
201110
201510
FIG. 1 — Lineage of K841788, 1985–2015Source: FDA 510(k) summaries, read by 510(k) Report · 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DRS? 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 DRS device

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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? (7)

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K070710Accutrans Disposable Pressure Monitoring SystemBiosensors International-USA20072
K991886Pulsion Pulsiocath, Pulsion Pcco Monitoring Kit, Pulsion in-Line Injectate SensorPulsion Medical Systems, Inc.20001
K101189Reavillmed Pressure Monitoring System and PiccReavillmed20100
K981745Biotrans Reusable Sensor Base Model Number BT XxxxxxSunscope Intl., Inc.19980

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, K070710 (Biosensors International-USA, 2007) has gone furthest, with 2 descendants of its own.

How does its category compare?

All DRS devices

DRS Transducer, Blood-Pressure, Extravascular: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DRS

1in 2025

2007: 12009: 22010: 22011: 32012: 12013: 12014: 12015: 12016: 32017: 22023: 12025: 12026 (partial year): 1
2007high 3 (2011) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DRS

186in 2016

2011: 135 days median2016: 186 days median
2007high 186 (2016) · low 135 (2011)2026

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

Recalls per year · DRS

15in 2023

2016: 1622018: 112023: 152026 (partial year): 2, 2 Class I
2007high 162 (2016) · low 0 (2007)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · DRS

187in 2025

2007: 3972008: 5312009: 3442010: 1152011: 632012: 432013: 392014: 232015: 602016: 892017: 922018: 822019: 842020: 412021: 932022: 952023: 1472024: 2052025: 187
2007high 531 (2008) · low 23 (2014)2025

MAUDE reports naming product code DRS, 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
20071—0397
20080—0531
20092—0344
20102—0115
20113135063
20121—043
20131—039
20141—023
20151—060
2016318616289
20172—092
20180—1182
20190—084
20200—041
20210—093
20220—095
20231—15147
20240—0205
20251—0187
20261—2 (2)—
Cite this page

510(k) Report. “K841788: Utah Disposable Pressure Transducer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K841788

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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