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FDA 510(k)

ELECTRO-CAUTERY SUCTION TUBE

K-Number: K881413 · 1988-04-21

ApplicantAlto Development Corp.
Decision Date1988-04-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRO-CAUTERY SUCTION TUBE 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 1988-04-21 under 510(k) number K881413. 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 ELECTRO-CAUTERY SUCTION TUBE?

ELECTRO-CAUTERY SUCTION TUBE is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Alto Development Corp.. The 510(k) number is K881413.

When did ELECTRO-CAUTERY SUCTION TUBE receive FDA 510(k) clearance?

ELECTRO-CAUTERY SUCTION TUBE received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881413.

Who is the listed applicant for ELECTRO-CAUTERY SUCTION TUBE?

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 ELECTRO-CAUTERY SUCTION TUBE?

The FDA product code for ELECTRO-CAUTERY SUCTION TUBE is GEI.

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Other records listing Alto Development Corp. 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.

K964621A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTONK932513LABELING FOR MYO/WIRE II STERNOTOMY SUTURESK931537A&E MEDICAL ELECTROSURG ELECTRO W/NON-STICK COATK930528A&E MEDICAL ELECTROSURGICAL CONNECTING CORDSK914193A&E MEDICAL CORP DISPOS SUCT COAG W/NON STICK COATK915300A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES

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Related Devices (Code: GEI)

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

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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