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FDA 510(k)

SILA CLEAN 20/20

K-Number: K832327 · 1984-07-09

ApplicantProfessional Supplies, Inc.
Decision Date1984-07-09
Product Code
DecisionSubstantially Equivalent

Device Summary

SILA CLEAN 20/20 is the device name listed in this FDA 510(k) record. The listed applicant is Professional Supplies, Inc.. It received FDA 510(k) clearance on 1984-07-09 under 510(k) number K832327. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILA CLEAN 20/20?

SILA CLEAN 20/20 is a medical device that received FDA 510(k) clearance on 1984-07-09. The listed applicant is Professional Supplies, Inc.. The 510(k) number is K832327.

When did SILA CLEAN 20/20 receive FDA 510(k) clearance?

SILA CLEAN 20/20 received FDA 510(k) clearance on 1984-07-09, under 510(k) number K832327.

Who is the listed applicant for SILA CLEAN 20/20?

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

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.

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Other records listing Professional Supplies, 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.

K850046PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE

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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