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)

VILA-COOKE(TM) ANESTHESIA PILLOW

K-Number: K932305 · 1993-10-05

ApplicantSharn, Inc.
Decision Date1993-10-05
Product CodeCCX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VILA-COOKE(TM) ANESTHESIA PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Sharn, Inc.. It received FDA 510(k) clearance on 1993-10-05 under 510(k) number K932305. The device is classified under product code CCX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VILA-COOKE(TM) ANESTHESIA PILLOW?

VILA-COOKE(TM) ANESTHESIA PILLOW is a medical device that received FDA 510(k) clearance on 1993-10-05. The listed applicant is Sharn, Inc.. The 510(k) number is K932305.

When did VILA-COOKE(TM) ANESTHESIA PILLOW receive FDA 510(k) clearance?

VILA-COOKE(TM) ANESTHESIA PILLOW received FDA 510(k) clearance on 1993-10-05, under 510(k) number K932305.

Who is the listed applicant for VILA-COOKE(TM) ANESTHESIA PILLOW?

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

What is the FDA product code for VILA-COOKE(TM) ANESTHESIA PILLOW?

The FDA product code for VILA-COOKE(TM) ANESTHESIA PILLOW is CCX.

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 Sharn, 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: CCX)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑