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FDA 510(k)

IL88640 & 88641 CASSETTE-TAPE PROGRAM

K-Number: K801131 · 1980-05-23

ApplicantInstrumentation Laboratory CO
Decision Date1980-05-23
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL88640 & 88641 CASSETTE-TAPE PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1980-05-23 under 510(k) number K801131. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL88640 & 88641 CASSETTE-TAPE PROGRAM?

IL88640 & 88641 CASSETTE-TAPE PROGRAM is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K801131.

When did IL88640 & 88641 CASSETTE-TAPE PROGRAM receive FDA 510(k) clearance?

IL88640 & 88641 CASSETTE-TAPE PROGRAM received FDA 510(k) clearance on 1980-05-23, under 510(k) number K801131.

Who is the listed applicant for IL88640 & 88641 CASSETTE-TAPE PROGRAM?

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

What is the FDA product code for IL88640 & 88641 CASSETTE-TAPE PROGRAM?

The FDA product code for IL88640 & 88641 CASSETTE-TAPE PROGRAM is JQP.

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Related Devices (Code: JQP)

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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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