NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)
K-Number: K872838 · 1987-08-25
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Device Summary
Frequently Asked Questions
What is the NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)?
NORFOLK NORPORT (TM) -SP (SKIN PARALLEL) is a medical device that received FDA 510(k) clearance on 1987-08-25. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K872838.
When did NORFOLK NORPORT (TM) -SP (SKIN PARALLEL) receive FDA 510(k) clearance?
NORFOLK NORPORT (TM) -SP (SKIN PARALLEL) received FDA 510(k) clearance on 1987-08-25, under 510(k) number K872838.
Who is the listed applicant for NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)?
The FDA 510(k) record lists Norfolk Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)?
The FDA product code for NORFOLK NORPORT (TM) -SP (SKIN PARALLEL) is LJT.
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 Norfolk Medical Products, 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: LJT)
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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