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)

SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM

K-Number: K870123 · 1987-02-04

ApplicantAvery Intl.
Decision Date1987-02-04
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM is the device name listed in this FDA 510(k) record. The listed applicant is Avery Intl.. It received FDA 510(k) clearance on 1987-02-04 under 510(k) number K870123. 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 SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM?

SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Avery Intl.. The 510(k) number is K870123.

When did SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM receive FDA 510(k) clearance?

SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM received FDA 510(k) clearance on 1987-02-04, under 510(k) number K870123.

Who is the listed applicant for SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM?

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

What is the FDA product code for SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM?

The FDA product code for SURGICAL DRAPES AND ACCESSORIES USING PCCE FILM 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 Avery Intl. 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.

View all 12 devices →

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

View on FDA Database →

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

↑