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FDA 510(k)

GLYDE DAM LOLLYES

K-Number: K970577 · 1998-01-08

ApplicantGlyde USA, Inc.
Decision Date1998-01-08
Product CodeMSC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GLYDE DAM LOLLYES is the device name listed in this FDA 510(k) record. The listed applicant is Glyde USA, Inc.. It received FDA 510(k) clearance on 1998-01-08 under 510(k) number K970577. 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 GLYDE DAM LOLLYES?

GLYDE DAM LOLLYES is a medical device that received FDA 510(k) clearance on 1998-01-08. The listed applicant is Glyde USA, Inc.. The 510(k) number is K970577.

When did GLYDE DAM LOLLYES receive FDA 510(k) clearance?

GLYDE DAM LOLLYES received FDA 510(k) clearance on 1998-01-08, under 510(k) number K970577.

Who is the listed applicant for GLYDE DAM LOLLYES?

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

What is the FDA product code for GLYDE DAM LOLLYES?

The FDA product code for GLYDE DAM LOLLYES 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.K990067SHEER GLYDE DAMSLouise C. Myers

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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