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FDA 510(k)

AMSCO STERILE RECOVERIES SURGICAL PACKS

K-Number: K932522 · 1994-09-09

ApplicantAmsco Sterile Recoveries, Inc.
Decision Date1994-09-09
Product CodeLRD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AMSCO STERILE RECOVERIES SURGICAL PACKS is the device name listed in this FDA 510(k) record. The listed applicant is Amsco Sterile Recoveries, Inc.. It received FDA 510(k) clearance on 1994-09-09 under 510(k) number K932522. The device is classified under product code LRD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSCO STERILE RECOVERIES SURGICAL PACKS?

AMSCO STERILE RECOVERIES SURGICAL PACKS is a medical device that received FDA 510(k) clearance on 1994-09-09. The listed applicant is Amsco Sterile Recoveries, Inc.. The 510(k) number is K932522.

When did AMSCO STERILE RECOVERIES SURGICAL PACKS receive FDA 510(k) clearance?

AMSCO STERILE RECOVERIES SURGICAL PACKS received FDA 510(k) clearance on 1994-09-09, under 510(k) number K932522.

Who is the listed applicant for AMSCO STERILE RECOVERIES SURGICAL PACKS?

The FDA 510(k) record lists Amsco Sterile Recoveries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMSCO STERILE RECOVERIES SURGICAL PACKS?

The FDA product code for AMSCO STERILE RECOVERIES SURGICAL PACKS is LRD.

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.

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Other records listing Amsco Sterile Recoveries, 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.

K931143AMSCO STERILE RECOVERIES ABSORBENT TOWELSK931146SURGICAL DRAPES, MODIFICATIONK931874RECOVERIES AUTOCLAVABLE RESUABLE WRAP -- FAC. USEK931145NON-STERILE ISOLATION GOWNK931144STERILE SURGEON'S GOWN, MODIFICATIONK931875AUTOCLAVABLE REUSABLE WRAP -- CENTERAL SERVICE USE

View all 12 devices →

Related Devices (Code: LRD)

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.

K984345AROMAPATCHEnvis, Inc.K942789MISTASSISTThe Merlin Corp.K940133THE EXPANDACELL EAR PACKDenver Splint Co.K925022SURGICAL TRAY (STERILE)Customed, Inc.K920842AEROSOL DELIVERY SYSTEMSHospitak, Inc.

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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