510(k) Report

FDA applicant

Minnesota Mining and Mfg. Co.

St. Paul, MN9 decisions1983–20023 recalls

FDA records 9 decisions for Minnesota Mining and Mfg. Co. (St. Paul, MN) from 1983 to 2002: 9 510(k) clearances. Most are in product codes JOJ (Indicator, Physical/Chemical Sterilization…) and FRN (Pump, Infusion). Its devices cite 6 predicates, 0 of them its own earlier devices. 3 recalls are linked to its devices.

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

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Minnesota Mining and Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Minnesota Mining and Mfg. Co. since 2007.

Recalls per year

2in 2008

2008: 2
2007high 2 (2008) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Minnesota Mining and Mfg. Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Minnesota Mining and Mfg. Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • JOJIndicator, Physical/Chemical Sterilization Process2decisions
  • FRNPump, Infusion1decision
  • FXXMask, Surgical1decision
  • DSACable, Transducer And Electrode, Patient, (Including Connector)1decision
  • EJRAgent, Polishing, Abrasive, Oral Cavity1decision
  • DQDStethoscope, Electronic1decision

Also: DRX (1).

Whose devices does it build on?

Its devices cite 6 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 9 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K9618483M Littmann Electronic StethoscopeMinnesota Mining and Mfg. Co. · 19975cite it
  • K0006903M Red Dot Radiolucent Monitoring Electrode with Conductive AdhesiveMinnesota Mining and Mfg. Co. · 20002cite it
  • K9904823M Clinpro Prophy Paste, Model 12611Minnesota Mining and Mfg. Co. · 19991cites it
  • K0132283M Comply 1248 Gas Plasma Chemical IndicatorMinnesota Mining and Mfg. Co. · 20021cites it

What has FDA decided for it lately?

  • K0132283M Comply 1248 Gas Plasma Chemical IndicatorMinnesota Mining and Mfg. Co. · 20021 recall
  • K0003553M Comply 1249 Liquid Peracetic Acid Chemical IndicatorMinnesota Mining and Mfg. Co. · 2000
  • K0006903M Red Dot Radiolucent Monitoring Electrode with Conductive AdhesiveMinnesota Mining and Mfg. Co. · 2000
  • K9904823M Clinpro Prophy Paste, Model 12611Minnesota Mining and Mfg. Co. · 1999
  • K9618483M Littmann Electronic StethoscopeMinnesota Mining and Mfg. Co. · 1997
  • K9650433M 1830 Fluid Block Anti-Fog Tie-on Surgical Mask and 3M 1830FS Fluid Block Anti-Fog Tie-on Surgical Mask…Minnesota Mining and Mfg. Co. · 1997
  • K9549003M Red Dot Ecg Lead Wires aMinnesota Mining and Mfg. Co. · 1996
  • K9404463M Model 3000 & Model 3100 Infusion Pump (Modification)Minnesota Mining and Mfg. Co. · 19942 recalls

All 9 as Minnesota Mining and Mfg. Co. →

What has been recalled?

3 recalls linked to its devices; the latest:

  • K940446Deltec 3000 Large Volume Infusion Pump, CE 0473, RX Only, Smiths Medical MD, Inc. 1265…Feb 27, 2008
  • K940446Deltec Micro 3100 Large Volume Infusion Pump, CE 0473, RX Only, Smiths Medical MD, Inc.…Feb 27, 2008
  • K0132283M Comply 1248 Gas Plasma Chemical Indicator Strips for use in STERRAD 100, STERRAD 100S…Aug 9, 2006

Other applicant names beginning “Minnesota”

FDA records each applicant name separately; these may or may not be the same firm.

Minnesota Laser Corp. 12Minnesota Scientific, Inc. 5Minnesota Valley Engineering, Inc. 4Minnesota Medical Development, Inc. 3Minnesota Prophy Power, Inc. 2Minnesota Resuscitation Solutions, D.B.D Advancedcpr… 1Minnesota Medical Technologies 1The Minnesota Back Brace Co. 1