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FDA 510(k)

SITE STRIP

K-Number: K843200 · 1985-03-12

ApplicantE-Med Corp.
Decision Date1985-03-12
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SITE STRIP is the device name listed in this FDA 510(k) record. The listed applicant is E-Med Corp.. It received FDA 510(k) clearance on 1985-03-12 under 510(k) number K843200. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SITE STRIP?

SITE STRIP is a medical device that received FDA 510(k) clearance on 1985-03-12. The listed applicant is E-Med Corp.. The 510(k) number is K843200.

When did SITE STRIP receive FDA 510(k) clearance?

SITE STRIP received FDA 510(k) clearance on 1985-03-12, under 510(k) number K843200.

Who is the listed applicant for SITE STRIP?

The FDA 510(k) record lists E-Med Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SITE STRIP?

The FDA product code for SITE STRIP is NAD.

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 E-Med Corp. 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: NAD)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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