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FDA 510(k)

MATRIX VIDEO IMAGER 1020 COMPACT CAMER

K-Number: K842495 · 1984-08-17

ApplicantMatrix Instruments
Decision Date1984-08-17
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MATRIX VIDEO IMAGER 1020 COMPACT CAMER is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Instruments. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842495. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIX VIDEO IMAGER 1020 COMPACT CAMER?

MATRIX VIDEO IMAGER 1020 COMPACT CAMER is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Matrix Instruments. The 510(k) number is K842495.

When did MATRIX VIDEO IMAGER 1020 COMPACT CAMER receive FDA 510(k) clearance?

MATRIX VIDEO IMAGER 1020 COMPACT CAMER received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842495.

Who is the listed applicant for MATRIX VIDEO IMAGER 1020 COMPACT CAMER?

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 VIDEO IMAGER 1020 COMPACT CAMER?

The FDA product code for MATRIX VIDEO IMAGER 1020 COMPACT CAMER is IZI.

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 DIGITIZERK860776MATRIX LR, LR 22A & LR/LASER RECORDERK842494MATRIS INSTRU. VIDEO IMAGER 1010-

Related Devices (Code: IZI)

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.

K261037780 nm SPY Portable Handheld Imaging (SPY-PHI) SystemStryker EndoscopyK253181SURGIMAGE SIM 1000H Fluorescence Imaging PlatformSurgimage CorporationK243645IC-Flow™ Imaging System 2.0Diagnostic Green GmbHK243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K231986Modus IRSynaptive Medical, Inc.K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision GmbH

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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