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FDA 510(k)

SOFT SUCTION ADAPTER

K-Number: K895684 · 1989-11-20

ApplicantApplied Medical Technologies
Decision Date1989-11-20
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOFT SUCTION ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technologies. It received FDA 510(k) clearance on 1989-11-20 under 510(k) number K895684. 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 SOFT SUCTION ADAPTER?

SOFT SUCTION ADAPTER is a medical device that received FDA 510(k) clearance on 1989-11-20. The listed applicant is Applied Medical Technologies. The 510(k) number is K895684.

When did SOFT SUCTION ADAPTER receive FDA 510(k) clearance?

SOFT SUCTION ADAPTER received FDA 510(k) clearance on 1989-11-20, under 510(k) number K895684.

Who is the listed applicant for SOFT SUCTION ADAPTER?

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

What is the FDA product code for SOFT SUCTION ADAPTER?

The FDA product code for SOFT SUCTION ADAPTER is GEA.

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Other records listing Applied Medical Technologies 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.

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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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