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FDA 510(k)

CAP, CLARION NURSES OR (TECHNIC)

K-Number: K770260 · 1977-03-07

Decision Date1977-03-07
Product CodeFYF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAP, CLARION NURSES OR (TECHNIC) is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1977-03-07 under 510(k) number K770260. The device is classified under product code FYF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAP, CLARION NURSES OR (TECHNIC)?

CAP, CLARION NURSES OR (TECHNIC) is a medical device that received FDA 510(k) clearance on 1977-03-07. The listed applicant is Sherwood Medical Industries. The 510(k) number is K770260.

When did CAP, CLARION NURSES OR (TECHNIC) receive FDA 510(k) clearance?

CAP, CLARION NURSES OR (TECHNIC) received FDA 510(k) clearance on 1977-03-07, under 510(k) number K770260.

Who is the listed applicant for CAP, CLARION NURSES OR (TECHNIC)?

The FDA 510(k) record lists Sherwood Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAP, CLARION NURSES OR (TECHNIC)?

The FDA product code for CAP, CLARION NURSES OR (TECHNIC) is FYF.

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 Sherwood Medical Industries 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 62 devices →

Related Devices (Code: FYF)

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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