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FDA 510(k)

'E' CUBE AND 'E' PAD

K-Number: K873916 · 1987-12-11

ApplicantRichmond Products, Inc.
Decision Date1987-12-11
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

'E' CUBE AND 'E' PAD is the device name listed in this FDA 510(k) record. The listed applicant is Richmond Products, Inc.. It received FDA 510(k) clearance on 1987-12-11 under 510(k) number K873916. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 'E' CUBE AND 'E' PAD?

'E' CUBE AND 'E' PAD is a medical device that received FDA 510(k) clearance on 1987-12-11. The listed applicant is Richmond Products, Inc.. The 510(k) number is K873916.

When did 'E' CUBE AND 'E' PAD receive FDA 510(k) clearance?

'E' CUBE AND 'E' PAD received FDA 510(k) clearance on 1987-12-11, under 510(k) number K873916.

Who is the listed applicant for 'E' CUBE AND 'E' PAD?

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

What is the FDA product code for 'E' CUBE AND 'E' PAD?

The FDA product code for 'E' CUBE AND 'E' PAD is HOX.

Other records listing Richmond Products, Inc. as applicant

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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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