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FDA 510(k)

TABLE, EXAMINATION

K-Number: K770437 · 1977-03-23

Decision Date1977-03-23
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TABLE, EXAMINATION is the device name listed in this FDA 510(k) record. The listed applicant is I E Industries. It received FDA 510(k) clearance on 1977-03-23 under 510(k) number K770437. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TABLE, EXAMINATION?

TABLE, EXAMINATION is a medical device that received FDA 510(k) clearance on 1977-03-23. The listed applicant is I E Industries. The 510(k) number is K770437.

When did TABLE, EXAMINATION receive FDA 510(k) clearance?

TABLE, EXAMINATION received FDA 510(k) clearance on 1977-03-23, under 510(k) number K770437.

Who is the listed applicant for TABLE, EXAMINATION?

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

What is the FDA product code for TABLE, EXAMINATION?

The FDA product code for TABLE, EXAMINATION is KNC.

Related Clinical Trials

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.

Other records listing I E Industries 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.

Related Devices (Code: KNC)

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.

Official Source

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