510(k) Report

510(k) · Cleared

Cleared

S.P.a.R Sterile Ambulatory Reservoir

K990091510(k) TraditionalCleared Apr 4, 199983-day reviewClass II21 CFR 880.5725

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

Faulding Pharmaceutical Co. · MRZ Accessories, Pump, Infusion

Cleared on Apr 4, 1999 as substantially equivalent to K843772 (Deltec Systems, Inc., 1984) after an 83-day review. Its family tree reaches back 1 generation to 1984.

Decided
Apr 4, 1999
Review
83 days
Class
Class II
Product code
MRZ
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K843772 (1984). No later device cites it as a predicate yet.

K843772 · Cadd-1 5100 Ambulatory Infusion Pump · Deltec Systems, Inc. · 1984 · recalled19801985199019952000
  1. Root · 1 generation backK843772 Cadd-1 5100 Ambulatory Infusion PumpDeltec Systems, Inc. · 1984 · Recalled
  2. This deviceK990091 S.P.a.R Sterile Ambulatory ReservoirFaulding Pharmaceutical Co. · 1999
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K843772Cadd-1 5100 Ambulatory Infusion PumpDeltec Systems, Inc.198412
0 (this device)K990091S.P.a.R Sterile Ambulatory ReservoirFaulding Pharmaceutical Co.1999—
FIG. 1 — Lineage of K990091, 1984–1999Source: 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), 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 MRZ? 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 MRZ device

  1. #1 K193654 BlueStar Rxscore 7.5 · 9 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? (1)

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
*K843772Cadd-1 5100 Ambulatory Infusion Pump
Summary page 1
…e: Medication Reservoir 3. Proprietary Name: S.P.A.R.™ sterile Ambulatory Reservoir 4. Classification: Class II 5. Predicate Device: SIMS Deltec Medication Cassette™™ (K843772) 6. Description of the Device: The S.P.A.R.™ Sterile Ambulatory Reservoir is a sterile, disposable, non- pyrogenic, tamper proof…
Deltec Systems, Inc.198412

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.

What does this lineage say?

  • Its one ancestor has a recall.

How does its category compare?

All MRZ devices

MRZ Accessories, Pump, Infusion: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MRZ

1in 2023

2007: 22008: 42009: 22010: 22011: 12012: 22013: 12014: 22015: 12016: 22017: 22018: 12019: 12020: 22021: 12022: 12023: 1
2007high 4 (2008) · low 0 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MRZ

96in 2008

2008: 96 days median
2007high 96 (2008)2026

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

Recalls per year · MRZ

5in 2019

2009: 12018: 12019: 5
2007high 5 (2019) · low 0 (2007)2026

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

Adverse event reports per year · MRZ

35in 2025

2011: 22012: 12015: 1172016: 552017: 182018: 462019: 362020: 442021: 612022: 392023: 272024: 412025: 35
2007high 117 (2015) · low 0 (2007)2025

MAUDE reports naming product code MRZ, 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
200849600
20092—10
20102—00
20111—02
20122—01
20131—00
20142—00
20151—0117
20162—055
20172—018
20181—146
20191—536
20202—044
20211—061
20221—039
20231—027
20240—041
20250—035
20260—0—

What is it indicated for?

The S.P.A.R.™ Sterile Ambulatory Reservoir is intended for use with the Sims Deltec CADD-PCA® Model 5800 and CADD-Prizm® Model 6100 Ambulatory Infusion Pumps, manufactured and distributed by Sims Deltec Inc., St. Paul, Minnesota. The S.P.A.R.™ Ambulatory Reservoir is intended for use as an accessory to the Sims Deltec CADD-PCA® Model 5800 and CADD-Prizm® Model 6100 infusion pumps by replacing the Deltec Medication Cassette ™, Model 2050 - 50 mL and 2100 - 100 mL with S.P.A.R. ™ Sterile Ambulatory Reservoir.

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. “K990091: S.P.a.R Sterile Ambulatory Reservoir.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K990091

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