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FDA 510(k)

MEDI-TRACE THERMAL VIDEO FILM PAPER

K-Number: K891192 · 1989-04-06

ApplicantGraphic Controls Corp.
Decision Date1989-04-06
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE THERMAL VIDEO FILM PAPER is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1989-04-06 under 510(k) number K891192. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-TRACE THERMAL VIDEO FILM PAPER?

MEDI-TRACE THERMAL VIDEO FILM PAPER is a medical device that received FDA 510(k) clearance on 1989-04-06. The listed applicant is Graphic Controls Corp.. The 510(k) number is K891192.

When did MEDI-TRACE THERMAL VIDEO FILM PAPER receive FDA 510(k) clearance?

MEDI-TRACE THERMAL VIDEO FILM PAPER received FDA 510(k) clearance on 1989-04-06, under 510(k) number K891192.

Who is the listed applicant for MEDI-TRACE THERMAL VIDEO FILM PAPER?

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

What is the FDA product code for MEDI-TRACE THERMAL VIDEO FILM PAPER?

The FDA product code for MEDI-TRACE THERMAL VIDEO FILM PAPER is LMD.

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Other records listing Graphic Controls Corp. 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.

K981964MEDI-TRACE 4103 NEONATAL ELECTRODEK983287MEDI-TRACE 1610C COMBINATION DEFIBRILLATION, MONITORING AND PACING ELECTRODEK974730SOFTRANS PLUS INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS PLUS IUPC)K980857MEDI-TRACE 1310P COMBINATION DEFIBRILLATION, MONITORING & PACING ELECTRODEK972970MEDI-TRACE 1510M COMBINATION DEFIBRILLATION, MONITORING AND PACING ELECTRODEK964387POINT OF USE II SHARPS-A-GATOR

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Related Devices (Code: LMD)

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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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