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FDA 510(k)

SURGICAL PLASTERS

K-Number: K861695 · 1986-08-01

ApplicantSalvaplast Industries
Decision Date1986-08-01
Product Code
DecisionSubstantially Equivalent

Device Summary

SURGICAL PLASTERS is the device name listed in this FDA 510(k) record. The listed applicant is Salvaplast Industries. It received FDA 510(k) clearance on 1986-08-01 under 510(k) number K861695. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL PLASTERS?

SURGICAL PLASTERS is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Salvaplast Industries. The 510(k) number is K861695.

When did SURGICAL PLASTERS receive FDA 510(k) clearance?

SURGICAL PLASTERS received FDA 510(k) clearance on 1986-08-01, under 510(k) number K861695.

Who is the listed applicant for SURGICAL PLASTERS?

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

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.

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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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