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FDA 510(k)

MULTIPLE STERILE SURGICAL DRAPE PACK

K-Number: K914605 · 1992-01-15

Decision Date1992-01-15
Product CodeKKX
Advisory CommitteeSU
DecisionUnknown

Device Summary

MULTIPLE STERILE SURGICAL DRAPE PACK is the device name listed in this FDA 510(k) record. The listed applicant is Assured Surgical Products, Inc.. It received FDA 510(k) clearance on 1992-01-15 under 510(k) number K914605. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MULTIPLE STERILE SURGICAL DRAPE PACK?

MULTIPLE STERILE SURGICAL DRAPE PACK is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is Assured Surgical Products, Inc.. The 510(k) number is K914605.

When did MULTIPLE STERILE SURGICAL DRAPE PACK receive FDA 510(k) clearance?

MULTIPLE STERILE SURGICAL DRAPE PACK received FDA 510(k) clearance on 1992-01-15, under 510(k) number K914605.

Who is the listed applicant for MULTIPLE STERILE SURGICAL DRAPE PACK?

The FDA 510(k) record lists Assured Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPLE STERILE SURGICAL DRAPE PACK?

The FDA product code for MULTIPLE STERILE SURGICAL DRAPE PACK is KKX.

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 Assured Surgical 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: KKX)

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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