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FDA 510(k)

CASSETTE TAPE REPLAY SYSTEM

K-Number: K870554 · 1987-03-23

ApplicantResearch Instrumentation Associates, Inc.
Decision Date1987-03-23
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CASSETTE TAPE REPLAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Research Instrumentation Associates, Inc.. It received FDA 510(k) clearance on 1987-03-23 under 510(k) number K870554. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CASSETTE TAPE REPLAY SYSTEM?

CASSETTE TAPE REPLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1987-03-23. The listed applicant is Research Instrumentation Associates, Inc.. The 510(k) number is K870554.

When did CASSETTE TAPE REPLAY SYSTEM receive FDA 510(k) clearance?

CASSETTE TAPE REPLAY SYSTEM received FDA 510(k) clearance on 1987-03-23, under 510(k) number K870554.

Who is the listed applicant for CASSETTE TAPE REPLAY SYSTEM?

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

What is the FDA product code for CASSETTE TAPE REPLAY SYSTEM?

The FDA product code for CASSETTE TAPE REPLAY SYSTEM is DSH.

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Related Devices (Code: DSH)

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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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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