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FDA 510(k)

SORBSAN TOPICAL WOUND DRESSING

K-Number: K881854 · 1988-07-19

Decision Date1988-07-19
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

SORBSAN TOPICAL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is E.G. Dick & Assoc.. It received FDA 510(k) clearance on 1988-07-19 under 510(k) number K881854. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORBSAN TOPICAL WOUND DRESSING?

SORBSAN TOPICAL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1988-07-19. The listed applicant is E.G. Dick & Assoc.. The 510(k) number is K881854.

When did SORBSAN TOPICAL WOUND DRESSING receive FDA 510(k) clearance?

SORBSAN TOPICAL WOUND DRESSING received FDA 510(k) clearance on 1988-07-19, under 510(k) number K881854.

Who is the listed applicant for SORBSAN TOPICAL WOUND DRESSING?

The FDA 510(k) record lists E.G. Dick & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORBSAN TOPICAL WOUND DRESSING?

The FDA product code for SORBSAN TOPICAL 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 E.G. Dick & Assoc. 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

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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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