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FDA 510(k)

SHEER GLYDE DAMS

K-Number: K990067 · 1999-02-19

ApplicantLouise C. Myers
Decision Date1999-02-19
Product CodeMSC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SHEER GLYDE DAMS is the device name listed in this FDA 510(k) record. The listed applicant is Louise C. Myers. It received FDA 510(k) clearance on 1999-02-19 under 510(k) number K990067. The device is classified under product code MSC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHEER GLYDE DAMS?

SHEER GLYDE DAMS is a medical device that received FDA 510(k) clearance on 1999-02-19. The listed applicant is Louise C. Myers. The 510(k) number is K990067.

When did SHEER GLYDE DAMS receive FDA 510(k) clearance?

SHEER GLYDE DAMS received FDA 510(k) clearance on 1999-02-19, under 510(k) number K990067.

Who is the listed applicant for SHEER GLYDE DAMS?

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

What is the FDA product code for SHEER GLYDE DAMS?

The FDA product code for SHEER GLYDE DAMS is MSC.

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Related Devices (Code: MSC)

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.

K253662LIXI (LXOSFM1)Luwi, LLCK212928LoralsBrazen Goods Inc. Dba LoralsK212037SancDam Latex Oral DamSanctuary Health Sdn. Bhd.K203727Harmony Latex Dam, Harmony Non-Latex DamPamco Distributing, Inc.K091769TRUST DAMLine One Laboratories, Inc.K970577GLYDE DAM LOLLYESGlyde USA, Inc.

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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