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FDA 510(k)

L-5 PLASTIC SURGERY CANNULAS

K-Number: K880669 · 1988-03-17

ApplicantAmerican Instrument Manufacturer'S, Inc.
Decision Date1988-03-17
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

L-5 PLASTIC SURGERY CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is American Instrument Manufacturer'S, Inc.. It received FDA 510(k) clearance on 1988-03-17 under 510(k) number K880669. 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 L-5 PLASTIC SURGERY CANNULAS?

L-5 PLASTIC SURGERY CANNULAS is a medical device that received FDA 510(k) clearance on 1988-03-17. The listed applicant is American Instrument Manufacturer'S, Inc.. The 510(k) number is K880669.

When did L-5 PLASTIC SURGERY CANNULAS receive FDA 510(k) clearance?

L-5 PLASTIC SURGERY CANNULAS received FDA 510(k) clearance on 1988-03-17, under 510(k) number K880669.

Who is the listed applicant for L-5 PLASTIC SURGERY CANNULAS?

The FDA 510(k) record lists American Instrument Manufacturer'S, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L-5 PLASTIC SURGERY CANNULAS?

The FDA product code for L-5 PLASTIC SURGERY CANNULAS is GEA.

Related Clinical Trials

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Other records listing American Instrument Manufacturer'S, Inc. 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.

K863163ULS 8-86

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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