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FDA 510(k)

COMPRESS AND SKULLCAP, HEAD DRESSING

K-Number: K870240 · 1987-02-20

ApplicantFraass Survival Systems, Inc.
Decision Date1987-02-20
Product CodeEXR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COMPRESS AND SKULLCAP, HEAD DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Fraass Survival Systems, Inc.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K870240. The device is classified under product code EXR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESS AND SKULLCAP, HEAD DRESSING?

COMPRESS AND SKULLCAP, HEAD DRESSING is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K870240.

When did COMPRESS AND SKULLCAP, HEAD DRESSING receive FDA 510(k) clearance?

COMPRESS AND SKULLCAP, HEAD DRESSING received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870240.

Who is the listed applicant for COMPRESS AND SKULLCAP, HEAD DRESSING?

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

What is the FDA product code for COMPRESS AND SKULLCAP, HEAD DRESSING?

The FDA product code for COMPRESS AND SKULLCAP, HEAD DRESSING is EXR.

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Other records listing Fraass Survival Systems, 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.

K912022FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZESK871458SURVIVAL KIT, INDIVIDUAL, TROP, TACTICAL AIR CREWK871434MEDICAL PACKET, INDIVIDUAL SURVIVAL KIT, AIRMAN'SK871437SURVIVAL KIT, INDIVIDUALK871916FRASTEC DRY BURN DRESSINGK871917FRASTEC DRY GAUZE BANDAGE

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Related Devices (Code: EXR)

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.

K934142URINARY DRAINAGE BAGKey Medical Services, Inc.K935578URINE METERPuritas Health Care, Inc.K911258KENDALL PEDIATRIC URINE METERKendall Healthcare Products Co. Div.Of Tyco HealthK896732UNOMETER 500Unoplast A/SK771561DOVER URINE METERWill Ross Co.K770939URINE TESTER, MODEL 701Brother Scientific Products, 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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