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)

ISOSIT C & B MATERIAL

K-Number: K810969 · 1981-05-05

Decision Date1981-05-05
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ISOSIT C & B MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Bauer, Cheng & Associates, Inc.. It received FDA 510(k) clearance on 1981-05-05 under 510(k) number K810969. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOSIT C & B MATERIAL?

ISOSIT C & B MATERIAL is a medical device that received FDA 510(k) clearance on 1981-05-05. The listed applicant is Bauer, Cheng & Associates, Inc.. The 510(k) number is K810969.

When did ISOSIT C & B MATERIAL receive FDA 510(k) clearance?

ISOSIT C & B MATERIAL received FDA 510(k) clearance on 1981-05-05, under 510(k) number K810969.

Who is the listed applicant for ISOSIT C & B MATERIAL?

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

What is the FDA product code for ISOSIT C & B MATERIAL?

The FDA product code for ISOSIT C & B MATERIAL is EBF.

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 Bauer, Cheng & Associates, 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.

View all 11 devices →

Related Devices (Code: EBF)

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.

↑