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FDA 510(k)

SKINNY CHIBA NEEDLE & TRAY

K-Number: K813337 · 1982-01-28

Decision Date1982-01-28
Product CodeFSH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKINNY CHIBA NEEDLE & TRAY is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1982-01-28 under 510(k) number K813337. The device is classified under product code FSH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKINNY CHIBA NEEDLE & TRAY?

SKINNY CHIBA NEEDLE & TRAY is a medical device that received FDA 510(k) clearance on 1982-01-28. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K813337.

When did SKINNY CHIBA NEEDLE & TRAY receive FDA 510(k) clearance?

SKINNY CHIBA NEEDLE & TRAY received FDA 510(k) clearance on 1982-01-28, under 510(k) number K813337.

Who is the listed applicant for SKINNY CHIBA NEEDLE & TRAY?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKINNY CHIBA NEEDLE & TRAY?

The FDA product code for SKINNY CHIBA NEEDLE & TRAY is FSH.

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 Pharmaseal Div. Ahsc 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 64 devices →

Related Devices (Code: FSH)

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.

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