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FDA 510(k)

STERILE SURGICAL PACK

K-Number: K904873 · 1991-08-29

Decision Date1991-08-29
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE SURGICAL PACK is the device name listed in this FDA 510(k) record. The listed applicant is Angelica Healthcare Services. It received FDA 510(k) clearance on 1991-08-29 under 510(k) number K904873. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE SURGICAL PACK?

STERILE SURGICAL PACK is a medical device that received FDA 510(k) clearance on 1991-08-29. The listed applicant is Angelica Healthcare Services. The 510(k) number is K904873.

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

STERILE SURGICAL PACK received FDA 510(k) clearance on 1991-08-29, under 510(k) number K904873.

Who is the listed applicant for STERILE SURGICAL PACK?

The FDA 510(k) record lists Angelica Healthcare Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE SURGICAL PACK?

The FDA product code for STERILE SURGICAL 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.

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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