STEAMLINE
K-Number: K895910 · 1990-08-22
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Device Summary
Frequently Asked Questions
What is the STEAMLINE?
STEAMLINE is a medical device that received FDA 510(k) clearance on 1990-08-22. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K895910.
When did STEAMLINE receive FDA 510(k) clearance?
STEAMLINE received FDA 510(k) clearance on 1990-08-22, under 510(k) number K895910.
Who is the listed applicant for STEAMLINE?
The FDA 510(k) record lists Propper Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STEAMLINE?
The FDA product code for STEAMLINE is JOJ.
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 Propper Mfg. Co., 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.
Related Devices (Code: JOJ)
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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