SUPERGEL/SUPPRESSED DUST
K-Number: K940402 · 1994-03-28
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Device Summary
Frequently Asked Questions
What is the SUPERGEL/SUPPRESSED DUST?
SUPERGEL/SUPPRESSED DUST is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K940402.
When did SUPERGEL/SUPPRESSED DUST receive FDA 510(k) clearance?
SUPERGEL/SUPPRESSED DUST received FDA 510(k) clearance on 1994-03-28, under 510(k) number K940402.
Who is the listed applicant for SUPERGEL/SUPPRESSED DUST?
The FDA 510(k) record lists Harry J. Bosworth Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUPERGEL/SUPPRESSED DUST?
The FDA product code for SUPERGEL/SUPPRESSED DUST is ELW.
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 Harry J. Bosworth Co. 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: ELW)
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
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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