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)

3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX

K-Number: K874086 · 1987-12-17

Applicant3M Company
Decision Date1987-12-17
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1987-12-17 under 510(k) number K874086. 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 3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX?

3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX is a medical device that received FDA 510(k) clearance on 1987-12-17. The listed applicant is 3M Company. The 510(k) number is K874086.

When did 3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX receive FDA 510(k) clearance?

3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX received FDA 510(k) clearance on 1987-12-17, under 510(k) number K874086.

Who is the listed applicant for 3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX?

The FDA product code for 3M BRAND LASER PROTECTION SURGICAL DRAPES, 88XX 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 3M Company 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 322 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.

↑