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FDA 510(k)

AUTOMATIC EXPOSURE CONTROL TYPE A3300

K-Number: K827525 · 1982-06-18

ApplicantAdvanced Instrument Development, Inc.
Decision Date1982-06-18
Product Code
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC EXPOSURE CONTROL TYPE A3300 is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Instrument Development, Inc.. It received FDA 510(k) clearance on 1982-06-18 under 510(k) number K827525. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC EXPOSURE CONTROL TYPE A3300?

AUTOMATIC EXPOSURE CONTROL TYPE A3300 is a medical device that received FDA 510(k) clearance on 1982-06-18. The listed applicant is Advanced Instrument Development, Inc.. The 510(k) number is K827525.

When did AUTOMATIC EXPOSURE CONTROL TYPE A3300 receive FDA 510(k) clearance?

AUTOMATIC EXPOSURE CONTROL TYPE A3300 received FDA 510(k) clearance on 1982-06-18, under 510(k) number K827525.

Who is the listed applicant for AUTOMATIC EXPOSURE CONTROL TYPE A3300?

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

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Other records listing Advanced Instrument Development, 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.

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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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