CURITY PERINEAL WARM PACK
K-Number: K810692 · 1981-03-26
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Device Summary
Frequently Asked Questions
What is the CURITY PERINEAL WARM PACK?
CURITY PERINEAL WARM PACK is a medical device that received FDA 510(k) clearance on 1981-03-26. The listed applicant is The Kendal Co.. The 510(k) number is K810692.
When did CURITY PERINEAL WARM PACK receive FDA 510(k) clearance?
CURITY PERINEAL WARM PACK received FDA 510(k) clearance on 1981-03-26, under 510(k) number K810692.
Who is the listed applicant for CURITY PERINEAL WARM PACK?
The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURITY PERINEAL WARM PACK?
The FDA product code for CURITY PERINEAL WARM PACK is IMD.
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 The Kendal 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: IMD)
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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