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FDA 510(k)

CLEANSE N BOND II

K-Number: K844134 · 1985-01-04

ApplicantLee Pharmaceuticals
Decision Date1985-01-04
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEANSE N BOND II is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1985-01-04 under 510(k) number K844134. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEANSE N BOND II?

CLEANSE N BOND II is a medical device that received FDA 510(k) clearance on 1985-01-04. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K844134.

When did CLEANSE N BOND II receive FDA 510(k) clearance?

CLEANSE N BOND II received FDA 510(k) clearance on 1985-01-04, under 510(k) number K844134.

Who is the listed applicant for CLEANSE N BOND II?

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

What is the FDA product code for CLEANSE N BOND II?

The FDA product code for CLEANSE N BOND II is DYH.

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Other records listing Lee Pharmaceuticals 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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