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FDA 510(k)

MATRIX LR, LR 22A & LR/LASER RECORDER

K-Number: K860776 · 1986-06-16

ApplicantMatrix Instruments
Decision Date1986-06-16
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MATRIX LR, LR 22A & LR/LASER RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Instruments. It received FDA 510(k) clearance on 1986-06-16 under 510(k) number K860776. 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 MATRIX LR, LR 22A & LR/LASER RECORDER?

MATRIX LR, LR 22A & LR/LASER RECORDER is a medical device that received FDA 510(k) clearance on 1986-06-16. The listed applicant is Matrix Instruments. The 510(k) number is K860776.

When did MATRIX LR, LR 22A & LR/LASER RECORDER receive FDA 510(k) clearance?

MATRIX LR, LR 22A & LR/LASER RECORDER received FDA 510(k) clearance on 1986-06-16, under 510(k) number K860776.

Who is the listed applicant for MATRIX LR, LR 22A & LR/LASER RECORDER?

The FDA 510(k) record lists Matrix Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MATRIX LR, LR 22A & LR/LASER RECORDER?

The FDA product code for MATRIX LR, LR 22A & LR/LASER RECORDER is LMC.

Related Clinical Trials

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.

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Other records listing Matrix Instruments 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.

K860777MATRIX LD & LD/LASER DIGITIZERK842495MATRIX VIDEO IMAGER 1020 COMPACT CAMERK842494MATRIS INSTRU. VIDEO IMAGER 1010-

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

View on FDA Database →

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

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