KALTOCARB WOUND DRESSING
K-Number: K894347 · 1989-08-23
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Device Summary
Frequently Asked Questions
What is the KALTOCARB WOUND DRESSING?
KALTOCARB WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1989-08-23. The listed applicant is Calgon Vestal Div.. The 510(k) number is K894347.
When did KALTOCARB WOUND DRESSING receive FDA 510(k) clearance?
KALTOCARB WOUND DRESSING received FDA 510(k) clearance on 1989-08-23, under 510(k) number K894347.
Who is the listed applicant for KALTOCARB WOUND DRESSING?
The FDA 510(k) record lists Calgon Vestal Div. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KALTOCARB WOUND DRESSING?
The FDA product code for KALTOCARB WOUND DRESSING is FRO. This falls under the Anesthesiology category.
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 Calgon Vestal Div. 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: FRO)
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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