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FDA 510(k)

SINTERLOY

K-Number: K873373 · 1987-10-27

ApplicantDenpac Corp.
Decision Date1987-10-27
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SINTERLOY is the device name listed in this FDA 510(k) record. The listed applicant is Denpac Corp.. It received FDA 510(k) clearance on 1987-10-27 under 510(k) number K873373. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINTERLOY?

SINTERLOY is a medical device that received FDA 510(k) clearance on 1987-10-27. The listed applicant is Denpac Corp.. The 510(k) number is K873373.

When did SINTERLOY receive FDA 510(k) clearance?

SINTERLOY received FDA 510(k) clearance on 1987-10-27, under 510(k) number K873373.

Who is the listed applicant for SINTERLOY?

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

What is the FDA product code for SINTERLOY?

The FDA product code for SINTERLOY is EJS.

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 Denpac 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: EJS)

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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