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FDA 510(k)

FRAZIER SUCTION INSTRUMENT-DISPOS

K-Number: K832636 · 1983-10-14

ApplicantPilling Co.
Decision Date1983-10-14
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FRAZIER SUCTION INSTRUMENT-DISPOS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832636. 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 FRAZIER SUCTION INSTRUMENT-DISPOS?

FRAZIER SUCTION INSTRUMENT-DISPOS is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Pilling Co.. The 510(k) number is K832636.

When did FRAZIER SUCTION INSTRUMENT-DISPOS receive FDA 510(k) clearance?

FRAZIER SUCTION INSTRUMENT-DISPOS received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832636.

Who is the listed applicant for FRAZIER SUCTION INSTRUMENT-DISPOS?

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

What is the FDA product code for FRAZIER SUCTION INSTRUMENT-DISPOS?

The FDA product code for FRAZIER SUCTION INSTRUMENT-DISPOS is GEA.

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Other records listing Pilling 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

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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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