PELVX GELLHORN VAGINAL PESSARY 603-608
K-Number: K002329 · 2000-09-18
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Device Summary
Frequently Asked Questions
What is the PELVX GELLHORN VAGINAL PESSARY 603-608?
PELVX GELLHORN VAGINAL PESSARY 603-608 is a medical device that received FDA 510(k) clearance on 2000-09-18. The listed applicant is Deschutes Medical Products, Inc.. The 510(k) number is K002329.
When did PELVX GELLHORN VAGINAL PESSARY 603-608 receive FDA 510(k) clearance?
PELVX GELLHORN VAGINAL PESSARY 603-608 received FDA 510(k) clearance on 2000-09-18, under 510(k) number K002329.
Who is the listed applicant for PELVX GELLHORN VAGINAL PESSARY 603-608?
The FDA 510(k) record lists Deschutes Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PELVX GELLHORN VAGINAL PESSARY 603-608?
The FDA product code for PELVX GELLHORN VAGINAL PESSARY 603-608 is HHW.
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 Deschutes Medical Products, Inc. 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: HHW)
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
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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