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)

ISO-SHIELD SALIVA ABSORBERS

K-Number: K771908 · 1977-11-07

Applicant3M Company
Decision Date1977-11-07
Product CodeKHR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ISO-SHIELD SALIVA ABSORBERS is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1977-11-07 under 510(k) number K771908. The device is classified under product code KHR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISO-SHIELD SALIVA ABSORBERS?

ISO-SHIELD SALIVA ABSORBERS is a medical device that received FDA 510(k) clearance on 1977-11-07. The listed applicant is 3M Company. The 510(k) number is K771908.

When did ISO-SHIELD SALIVA ABSORBERS receive FDA 510(k) clearance?

ISO-SHIELD SALIVA ABSORBERS received FDA 510(k) clearance on 1977-11-07, under 510(k) number K771908.

Who is the listed applicant for ISO-SHIELD SALIVA ABSORBERS?

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 ISO-SHIELD SALIVA ABSORBERS?

The FDA product code for ISO-SHIELD SALIVA ABSORBERS is KHR.

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: KHR)

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.

↑