ROBISON & SMITH SURGICAL PACKS
K-Number: K955586 · 1996-08-30
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Device Summary
Frequently Asked Questions
What is the ROBISON & SMITH SURGICAL PACKS?
ROBISON & SMITH SURGICAL PACKS is a medical device that received FDA 510(k) clearance on 1996-08-30. The listed applicant is Robison & Smith, Inc.. The 510(k) number is K955586.
When did ROBISON & SMITH SURGICAL PACKS receive FDA 510(k) clearance?
ROBISON & SMITH SURGICAL PACKS received FDA 510(k) clearance on 1996-08-30, under 510(k) number K955586.
Who is the listed applicant for ROBISON & SMITH SURGICAL PACKS?
The FDA 510(k) record lists Robison & Smith, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROBISON & SMITH SURGICAL PACKS?
The FDA product code for ROBISON & SMITH SURGICAL PACKS is FYA.
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.
Related Devices (Code: FYA)
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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