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FDA 510(k)

ELECTRIC SELF STERILIZATION INOCUL. LOOP

K-Number: K813523 · 1981-12-31

ApplicantTechhnilab Instruments, Inc.
Decision Date1981-12-31
Product CodeLTB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTRIC SELF STERILIZATION INOCUL. LOOP is the device name listed in this FDA 510(k) record. The listed applicant is Techhnilab Instruments, Inc.. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813523. The device is classified under product code LTB. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC SELF STERILIZATION INOCUL. LOOP?

ELECTRIC SELF STERILIZATION INOCUL. LOOP is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Techhnilab Instruments, Inc.. The 510(k) number is K813523.

When did ELECTRIC SELF STERILIZATION INOCUL. LOOP receive FDA 510(k) clearance?

ELECTRIC SELF STERILIZATION INOCUL. LOOP received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813523.

Who is the listed applicant for ELECTRIC SELF STERILIZATION INOCUL. LOOP?

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

What is the FDA product code for ELECTRIC SELF STERILIZATION INOCUL. LOOP?

The FDA product code for ELECTRIC SELF STERILIZATION INOCUL. LOOP is LTB.

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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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