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FDA 510(k)

CONTAC CASE

K-Number: K863846 · 1987-04-06

ApplicantS. M. C. Medi-Tech Corp.
Decision Date1987-04-06
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONTAC CASE is the device name listed in this FDA 510(k) record. The listed applicant is S. M. C. Medi-Tech Corp.. It received FDA 510(k) clearance on 1987-04-06 under 510(k) number K863846. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTAC CASE?

CONTAC CASE is a medical device that received FDA 510(k) clearance on 1987-04-06. The listed applicant is S. M. C. Medi-Tech Corp.. The 510(k) number is K863846.

When did CONTAC CASE receive FDA 510(k) clearance?

CONTAC CASE received FDA 510(k) clearance on 1987-04-06, under 510(k) number K863846.

Who is the listed applicant for CONTAC CASE?

The FDA 510(k) record lists S. M. C. Medi-Tech Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTAC CASE?

The FDA product code for CONTAC CASE is LPN.

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Other records listing S. M. C. Medi-Tech 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.

K871130CONTACT LENS TWEEZERS

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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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