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FDA 510(k)

SKIN TECH. SURGI-STRIPS

K-Number: K833258 · 1984-01-25

ApplicantLee Tec Corp.
Decision Date1984-01-25
Product CodeFPX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SKIN TECH. SURGI-STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Lee Tec Corp.. It received FDA 510(k) clearance on 1984-01-25 under 510(k) number K833258. The device is classified under product code FPX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIN TECH. SURGI-STRIPS?

SKIN TECH. SURGI-STRIPS is a medical device that received FDA 510(k) clearance on 1984-01-25. The listed applicant is Lee Tec Corp.. The 510(k) number is K833258.

When did SKIN TECH. SURGI-STRIPS receive FDA 510(k) clearance?

SKIN TECH. SURGI-STRIPS received FDA 510(k) clearance on 1984-01-25, under 510(k) number K833258.

Who is the listed applicant for SKIN TECH. SURGI-STRIPS?

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

What is the FDA product code for SKIN TECH. SURGI-STRIPS?

The FDA product code for SKIN TECH. SURGI-STRIPS is FPX.

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Related Devices (Code: FPX)

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.

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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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