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FDA 510(k)

EURO TECH STERLING ROLLER TABLE

K-Number: K943973 · 1994-09-29

Decision Date1994-09-29
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EURO TECH STERLING ROLLER TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Electrical Therapeutics. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K943973. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EURO TECH STERLING ROLLER TABLE?

EURO TECH STERLING ROLLER TABLE is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Progressive Electrical Therapeutics. The 510(k) number is K943973.

When did EURO TECH STERLING ROLLER TABLE receive FDA 510(k) clearance?

EURO TECH STERLING ROLLER TABLE received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943973.

Who is the listed applicant for EURO TECH STERLING ROLLER TABLE?

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

What is the FDA product code for EURO TECH STERLING ROLLER TABLE?

The FDA product code for EURO TECH STERLING ROLLER TABLE is JFB.

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 Progressive Electrical Therapeutics 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 10 devices →

Related Devices (Code: JFB)

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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