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FDA 510(k)

TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM

K-Number: K915297 · 1992-02-11

ApplicantLifeguard Medical Products, Inc.
Decision Date1992-02-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM is the device name listed in this FDA 510(k) record. The listed applicant is Lifeguard Medical Products, Inc.. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K915297. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM?

TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Lifeguard Medical Products, Inc.. The 510(k) number is K915297.

When did TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM receive FDA 510(k) clearance?

TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM received FDA 510(k) clearance on 1992-02-11, under 510(k) number K915297.

Who is the listed applicant for TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM?

The FDA 510(k) record lists Lifeguard Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM?

The FDA product code for TROCAR & TROCAR SLEEEVE 11MM, 10MM, 8MM & 5MM is HET.

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Other records listing Lifeguard Medical Products, 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.

K013421LIFEGUARD NASAL CPAP MASK AND ACCESSORIESK915296MONOPOLAR ELECTRODEK920471LEVY ARTICULATING RETRACTORK915505REGULATOR FLOWMETERK915298SUCTION/IRRIGATION CANNULA; CATLOG #532.00K880958LIFEGUARD BACTERIAL AND VIRAL FILTER

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Related Devices (Code: HET)

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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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