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FDA 510(k)

CHIBA, MADAYAG, POTTS-COURNAND, SELDINGER BIOPSY N

K-Number: K853623 · 1985-10-08

ApplicantCo-Medical, Inc.
Decision Date1985-10-08
Product Code
DecisionSubstantially Equivalent

Device Summary

CHIBA, MADAYAG, POTTS-COURNAND, SELDINGER BIOPSY N is the device name listed in this FDA 510(k) record. The listed applicant is Co-Medical, Inc.. It received FDA 510(k) clearance on 1985-10-08 under 510(k) number K853623. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHIBA, MADAYAG, POTTS-COURNAND, SELDINGER BIOPSY N?

CHIBA, MADAYAG, POTTS-COURNAND, SELDINGER BIOPSY N is a medical device that received FDA 510(k) clearance on 1985-10-08. The listed applicant is Co-Medical, Inc.. The 510(k) number is K853623.

When did CHIBA, MADAYAG, POTTS-COURNAND, SELDINGER BIOPSY N receive FDA 510(k) clearance?

CHIBA, MADAYAG, POTTS-COURNAND, SELDINGER BIOPSY N received FDA 510(k) clearance on 1985-10-08, under 510(k) number K853623.

Who is the listed applicant for CHIBA, MADAYAG, POTTS-COURNAND, SELDINGER BIOPSY N?

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

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.

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Other records listing Co-Medical, 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.

K854003STERILE SOFT TISSUE BIOPSY NEEDLE

Official Source

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

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