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FDA 510(k)

MICRO-ID

K-Number: K760790 · 1976-10-29

ApplicantGeneral Diagnostics
Decision Date1976-10-29
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICRO-ID is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1976-10-29 under 510(k) number K760790. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-ID?

MICRO-ID is a medical device that received FDA 510(k) clearance on 1976-10-29. The listed applicant is General Diagnostics. The 510(k) number is K760790.

When did MICRO-ID receive FDA 510(k) clearance?

MICRO-ID received FDA 510(k) clearance on 1976-10-29, under 510(k) number K760790.

Who is the listed applicant for MICRO-ID?

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

What is the FDA product code for MICRO-ID?

The FDA product code for MICRO-ID is JSS.

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Other records listing General Diagnostics as applicant

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Related Devices (Code: JSS)

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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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