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FDA 510(k)

CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8

K-Number: K872808 · 1987-08-04

Decision Date1987-08-04
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8 is the device name listed in this FDA 510(k) record. The listed applicant is American Silk Sutures, Inc.. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K872808. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8?

CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8 is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is American Silk Sutures, Inc.. The 510(k) number is K872808.

When did CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8 receive FDA 510(k) clearance?

CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8 received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872808.

Who is the listed applicant for CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8?

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

What is the FDA product code for CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8?

The FDA product code for CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8 is EFQ.

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 American Silk Sutures, 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 14 devices →

Related Devices (Code: EFQ)

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

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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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