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FDA 510(k)

3M 1152 LASER IMAGER

K-Number: K936152 · 1994-09-21

Applicant3M Information,Imaging and Electronic Sector
Decision Date1994-09-21
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3M 1152 LASER IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is 3M Information,Imaging and Electronic Sector. It received FDA 510(k) clearance on 1994-09-21 under 510(k) number K936152. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M 1152 LASER IMAGER?

3M 1152 LASER IMAGER is a medical device that received FDA 510(k) clearance on 1994-09-21. The listed applicant is 3M Information,Imaging and Electronic Sector. The 510(k) number is K936152.

When did 3M 1152 LASER IMAGER receive FDA 510(k) clearance?

3M 1152 LASER IMAGER received FDA 510(k) clearance on 1994-09-21, under 510(k) number K936152.

Who is the listed applicant for 3M 1152 LASER IMAGER?

The FDA 510(k) record lists 3M Information,Imaging and Electronic Sector as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M 1152 LASER IMAGER?

The FDA product code for 3M 1152 LASER IMAGER is LMC.

Related Clinical Trials

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Other records listing 3M Information,Imaging and Electronic Sector as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K9361423M 1154 LASER IMAGERK9361533M 1156 MULTI-INPUT SYSTEM

Related Devices (Code: LMC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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