Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NON-LINTING DELIVERY BLANKET

K-Number: K932035 · 1994-05-26

ApplicantAmsco Sterile Recoveries, Inc.
Decision Date1994-05-26
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NON-LINTING DELIVERY BLANKET 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 1994-05-26 under 510(k) number K932035. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-LINTING DELIVERY BLANKET?

NON-LINTING DELIVERY BLANKET is a medical device that received FDA 510(k) clearance on 1994-05-26. The listed applicant is Amsco Sterile Recoveries, Inc.. The 510(k) number is K932035.

When did NON-LINTING DELIVERY BLANKET receive FDA 510(k) clearance?

NON-LINTING DELIVERY BLANKET received FDA 510(k) clearance on 1994-05-26, under 510(k) number K932035.

Who is the listed applicant for NON-LINTING DELIVERY BLANKET?

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 NON-LINTING DELIVERY BLANKET?

The FDA product code for NON-LINTING DELIVERY BLANKET is KNC.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K932522AMSCO STERILE RECOVERIES SURGICAL PACKSK931143AMSCO STERILE RECOVERIES ABSORBENT TOWELSK931146SURGICAL DRAPES, MODIFICATIONK931145NON-STERILE ISOLATION GOWNK931874RECOVERIES AUTOCLAVABLE RESUABLE WRAP -- FAC. USEK931875AUTOCLAVABLE REUSABLE WRAP -- CENTERAL SERVICE USE

View all 12 devices →

Related Devices (Code: KNC)

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.

K001261L720 EXAMINATION CHAIRLuneau Gynecologie SAK924420MEDICAL DISPOSABLE BEDDINGHill-Rom, Inc.K914544BD6000 THE OPTIMA & BD5000 BIRTHING BEDLic Care, Inc.K915779AFFINITY BED MODEL 3600 SERIESHill-Rom, Inc.K903973GARDOSI BIRTHING CUSHIONGraphic Controls Corp.K884868OBSTETRICAL SAFETY SYSTEMBuckman Co., 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.

↑