LOWENSTEIN-JENSEN SLANT
K-Number: K880123 · 1988-03-31
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Device Summary
Frequently Asked Questions
What is the LOWENSTEIN-JENSEN SLANT?
LOWENSTEIN-JENSEN SLANT is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Hardy Media. The 510(k) number is K880123.
When did LOWENSTEIN-JENSEN SLANT receive FDA 510(k) clearance?
LOWENSTEIN-JENSEN SLANT received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880123.
Who is the listed applicant for LOWENSTEIN-JENSEN SLANT?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOWENSTEIN-JENSEN SLANT?
The FDA product code for LOWENSTEIN-JENSEN SLANT is JSJ.
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 Hardy Media 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: JSJ)
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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