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FDA 510(k)

ENDOPATH VERESS NEEDLE

K-Number: K910855 · 1991-04-18

ApplicantSymbiosis Corp.
Decision Date1991-04-18
Product CodeFHP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH VERESS NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1991-04-18 under 510(k) number K910855. The device is classified under product code FHP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPATH VERESS NEEDLE?

ENDOPATH VERESS NEEDLE is a medical device that received FDA 510(k) clearance on 1991-04-18. The listed applicant is Symbiosis Corp.. The 510(k) number is K910855.

When did ENDOPATH VERESS NEEDLE receive FDA 510(k) clearance?

ENDOPATH VERESS NEEDLE received FDA 510(k) clearance on 1991-04-18, under 510(k) number K910855.

Who is the listed applicant for ENDOPATH VERESS NEEDLE?

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

What is the FDA product code for ENDOPATH VERESS NEEDLE?

The FDA product code for ENDOPATH VERESS NEEDLE is FHP.

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Other records listing Symbiosis 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.

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESK952432SYMBIOSIS BIPOLAR FORCEPSK951387SYMBIOSIS BIPOLAR SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORS

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Related Devices (Code: FHP)

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.

K860102MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLEEndotherapeutics

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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