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FDA 510(k)

CART, PROCEDURES

K-Number: K770438 · 1977-07-01

ApplicantI E Industries
Decision Date1977-07-01
Product CodeHDD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CART, PROCEDURES 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 1977-07-01 under 510(k) number K770438. The device is classified under product code HDD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CART, PROCEDURES?

CART, PROCEDURES is a medical device that received FDA 510(k) clearance on 1977-07-01. The listed applicant is I E Industries. The 510(k) number is K770438.

When did CART, PROCEDURES receive FDA 510(k) clearance?

CART, PROCEDURES received FDA 510(k) clearance on 1977-07-01, under 510(k) number K770438.

Who is the listed applicant for CART, PROCEDURES?

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 CART, PROCEDURES?

The FDA product code for CART, PROCEDURES is HDD.

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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.

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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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