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FDA 510(k)

MULAR GOLD LEAF ELECTRODE MODEL 7501

K-Number: K781476 · 1978-11-15

ApplicantLife-Tech Instruments, Inc.
Decision Date1978-11-15
Product CodeHLZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULAR GOLD LEAF ELECTRODE MODEL 7501 is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Instruments, Inc.. It received FDA 510(k) clearance on 1978-11-15 under 510(k) number K781476. The device is classified under product code HLZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULAR GOLD LEAF ELECTRODE MODEL 7501?

MULAR GOLD LEAF ELECTRODE MODEL 7501 is a medical device that received FDA 510(k) clearance on 1978-11-15. The listed applicant is Life-Tech Instruments, Inc.. The 510(k) number is K781476.

When did MULAR GOLD LEAF ELECTRODE MODEL 7501 receive FDA 510(k) clearance?

MULAR GOLD LEAF ELECTRODE MODEL 7501 received FDA 510(k) clearance on 1978-11-15, under 510(k) number K781476.

Who is the listed applicant for MULAR GOLD LEAF ELECTRODE MODEL 7501?

The FDA 510(k) record lists Life-Tech Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULAR GOLD LEAF ELECTRODE MODEL 7501?

The FDA product code for MULAR GOLD LEAF ELECTRODE MODEL 7501 is HLZ.

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Other records listing Life-Tech Instruments, Inc. 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.

K812177LIFE-TECH #1857 PRESSURE/POLOT MODULEK812179LIFE-TECH #1753 BIOFEEDBACK TRAINERK812180LIFE-TECH #5102 VISULABK812178LIFE-TECH #'S 1106/1156 UROLABSK800112AMBLYOPIA TRAINERK790663MODEL 1750 STANDING URINAL

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Related Devices (Code: HLZ)

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.

K253586RM Electrode (RMH 25-01)Retmap, Inc.K232273RM Electrode (RMH 23-01)Retmap, Inc.K961805TOMEY DTL ELECTRODETomey Corporation USAK926540SOPHER AND BIERER OVUM FORCEPSThomasville Medical Assoc.K913239GOLDLENS(TM)Doran Instruments, Inc.K844409DTL ELECTRODESauquoit Industries, Inc.

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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