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FDA 510(k)

SURETY COLUMN

K-Number: K802209 · 1980-10-23

ApplicantScientific Specialties, Inc.
Decision Date1980-10-23
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SURETY COLUMN is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Specialties, Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802209. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURETY COLUMN?

SURETY COLUMN is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Scientific Specialties, Inc.. The 510(k) number is K802209.

When did SURETY COLUMN receive FDA 510(k) clearance?

SURETY COLUMN received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802209.

Who is the listed applicant for SURETY COLUMN?

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

What is the FDA product code for SURETY COLUMN?

The FDA product code for SURETY COLUMN is JKA.

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Other records listing Scientific Specialties, 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.

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Related Devices (Code: JKA)

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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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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