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)

COLORED CASTING TAPE (RED AND BLUE)

K-Number: K870404 · 1987-02-13

Decision Date1987-02-13
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COLORED CASTING TAPE (RED AND BLUE) is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1987-02-13 under 510(k) number K870404. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLORED CASTING TAPE (RED AND BLUE)?

COLORED CASTING TAPE (RED AND BLUE) is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Buckman Co., Inc.. The 510(k) number is K870404.

When did COLORED CASTING TAPE (RED AND BLUE) receive FDA 510(k) clearance?

COLORED CASTING TAPE (RED AND BLUE) received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870404.

Who is the listed applicant for COLORED CASTING TAPE (RED AND BLUE)?

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

What is the FDA product code for COLORED CASTING TAPE (RED AND BLUE)?

The FDA product code for COLORED CASTING TAPE (RED AND BLUE) is LGF.

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 Buckman Co., 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 111 devices →

Related Devices (Code: LGF)

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.

↑