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FDA 510(k)

ATTENUATING SURGICAL GLOVE

K-Number: K891315 · 1989-10-05

ApplicantF & L Medical Products Co.
Decision Date1989-10-05
Product CodeLZC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ATTENUATING SURGICAL GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is F & L Medical Products Co.. It received FDA 510(k) clearance on 1989-10-05 under 510(k) number K891315. The device is classified under product code LZC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATTENUATING SURGICAL GLOVE?

ATTENUATING SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 1989-10-05. The listed applicant is F & L Medical Products Co.. The 510(k) number is K891315.

When did ATTENUATING SURGICAL GLOVE receive FDA 510(k) clearance?

ATTENUATING SURGICAL GLOVE received FDA 510(k) clearance on 1989-10-05, under 510(k) number K891315.

Who is the listed applicant for ATTENUATING SURGICAL GLOVE?

The FDA 510(k) record lists F & L Medical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATTENUATING SURGICAL GLOVE?

The FDA product code for ATTENUATING SURGICAL GLOVE is LZC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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