FDA 510(k)

A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON

K-Number: K964621 · 1996-12-20

Decision Date1996-12-20

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON is the device name listed in this FDA 510(k) record. The listed applicant is Alto Development Corp.. It received FDA 510(k) clearance on 1996-12-20 under 510(k) number K964621. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON?

A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON is a medical device that received FDA 510(k) clearance on 1996-12-20. The listed applicant is Alto Development Corp.. The 510(k) number is K964621.

When did A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON receive FDA 510(k) clearance?

A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON received FDA 510(k) clearance on 1996-12-20, under 510(k) number K964621.

Who is the listed applicant for A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON?

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

What is the FDA product code for A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON?

The FDA product code for A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON is GEI.

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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.