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FDA 510(k)

PLASTIC SUCTION TIPS

K-Number: K832521 · 1983-10-20

ApplicantWells Johnson Co.
Decision Date1983-10-20
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PLASTIC SUCTION TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Wells Johnson Co.. It received FDA 510(k) clearance on 1983-10-20 under 510(k) number K832521. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC SUCTION TIPS?

PLASTIC SUCTION TIPS is a medical device that received FDA 510(k) clearance on 1983-10-20. The listed applicant is Wells Johnson Co.. The 510(k) number is K832521.

When did PLASTIC SUCTION TIPS receive FDA 510(k) clearance?

PLASTIC SUCTION TIPS received FDA 510(k) clearance on 1983-10-20, under 510(k) number K832521.

Who is the listed applicant for PLASTIC SUCTION TIPS?

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

What is the FDA product code for PLASTIC SUCTION TIPS?

The FDA product code for PLASTIC SUCTION TIPS is GEA.

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Other records listing Wells Johnson Co. 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.

K991437WELLS JOHNSON INFUSION SYSTEM, MODEL 20-6000-00K984448BIRCOLL BALLOON DISSECTORK971580UAS ULTRASONIC ASPIRATOR SYSTEMK945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTK945500WELLS JOHNSON FIXATION SYSTEMK951519WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT

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Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, Inc.

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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