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FDA 510(k)

SECURIPIN

K-Number: K844457 · 1984-12-27

ApplicantHughes Int'L, Inc.
Decision Date1984-12-27
Product CodeEBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SECURIPIN is the device name listed in this FDA 510(k) record. The listed applicant is Hughes Int'L, Inc.. It received FDA 510(k) clearance on 1984-12-27 under 510(k) number K844457. The device is classified under product code EBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECURIPIN?

SECURIPIN is a medical device that received FDA 510(k) clearance on 1984-12-27. The listed applicant is Hughes Int'L, Inc.. The 510(k) number is K844457.

When did SECURIPIN receive FDA 510(k) clearance?

SECURIPIN received FDA 510(k) clearance on 1984-12-27, under 510(k) number K844457.

Who is the listed applicant for SECURIPIN?

The FDA 510(k) record lists Hughes Int'L, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SECURIPIN?

The FDA product code for SECURIPIN is EBL.

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Related Devices (Code: EBL)

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

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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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