OR SPECIALTIES VAGINAL PACK
K-Number: K820195 · 1982-03-05
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Device Summary
Frequently Asked Questions
What is the OR SPECIALTIES VAGINAL PACK?
OR SPECIALTIES VAGINAL PACK is a medical device that received FDA 510(k) clearance on 1982-03-05. The listed applicant is Howard Medical Co.. The 510(k) number is K820195.
When did OR SPECIALTIES VAGINAL PACK receive FDA 510(k) clearance?
OR SPECIALTIES VAGINAL PACK received FDA 510(k) clearance on 1982-03-05, under 510(k) number K820195.
Who is the listed applicant for OR SPECIALTIES VAGINAL PACK?
The FDA 510(k) record lists Howard Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OR SPECIALTIES VAGINAL PACK?
The FDA product code for OR SPECIALTIES VAGINAL PACK is EFQ.
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 Howard Medical Co. 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: EFQ)
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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