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FDA 510(k)

LECITHIN-SPINGOMYELIN STAND. & KITS

K-Number: K810743 · 1981-03-31

ApplicantSupelco, Inc.
Decision Date1981-03-31
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LECITHIN-SPINGOMYELIN STAND. & KITS is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1981-03-31 under 510(k) number K810743. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LECITHIN-SPINGOMYELIN STAND. & KITS?

LECITHIN-SPINGOMYELIN STAND. & KITS is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is Supelco, Inc.. The 510(k) number is K810743.

When did LECITHIN-SPINGOMYELIN STAND. & KITS receive FDA 510(k) clearance?

LECITHIN-SPINGOMYELIN STAND. & KITS received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810743.

Who is the listed applicant for LECITHIN-SPINGOMYELIN STAND. & KITS?

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

What is the FDA product code for LECITHIN-SPINGOMYELIN STAND. & KITS?

The FDA product code for LECITHIN-SPINGOMYELIN STAND. & KITS is JIS.

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Other records listing Supelco, Inc. as applicant

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Related Devices (Code: JIS)

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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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