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FDA 510(k)

DIGIFLEX SURGICAL GLOVES

K-Number: K972277 · 1997-10-21

Decision Date1997-10-21
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DIGIFLEX SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Hms Services, Inc.. It received FDA 510(k) clearance on 1997-10-21 under 510(k) number K972277. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGIFLEX SURGICAL GLOVES?

DIGIFLEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1997-10-21. The listed applicant is Hms Services, Inc.. The 510(k) number is K972277.

When did DIGIFLEX SURGICAL GLOVES receive FDA 510(k) clearance?

DIGIFLEX SURGICAL GLOVES received FDA 510(k) clearance on 1997-10-21, under 510(k) number K972277.

Who is the listed applicant for DIGIFLEX SURGICAL GLOVES?

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

What is the FDA product code for DIGIFLEX SURGICAL GLOVES?

The FDA product code for DIGIFLEX SURGICAL GLOVES is KGO.

Related Clinical Trials

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.

Related Devices (Code: KGO)

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.

Official Source

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