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FDA 510(k)

THE SS-99

K-Number: K943399 · 1994-09-16

ApplicantInstantron
Decision Date1994-09-16
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE SS-99 is the device name listed in this FDA 510(k) record. The listed applicant is Instantron. It received FDA 510(k) clearance on 1994-09-16 under 510(k) number K943399. The device is classified under product code KCW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SS-99?

THE SS-99 is a medical device that received FDA 510(k) clearance on 1994-09-16. The listed applicant is Instantron. The 510(k) number is K943399.

When did THE SS-99 receive FDA 510(k) clearance?

THE SS-99 received FDA 510(k) clearance on 1994-09-16, under 510(k) number K943399.

Who is the listed applicant for THE SS-99?

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

What is the FDA product code for THE SS-99?

The FDA product code for THE SS-99 is KCW.

Other records listing Instantron 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 7 devices →

Related Devices (Code: KCW)

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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