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FDA 510(k)

HEMOSTAT

K-Number: K770158 · 1977-01-31

ApplicantDeringer-Ney, Inc.
Decision Date1977-01-31
Product CodeEMD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HEMOSTAT is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1977-01-31 under 510(k) number K770158. The device is classified under product code EMD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOSTAT?

HEMOSTAT is a medical device that received FDA 510(k) clearance on 1977-01-31. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K770158.

When did HEMOSTAT receive FDA 510(k) clearance?

HEMOSTAT received FDA 510(k) clearance on 1977-01-31, under 510(k) number K770158.

Who is the listed applicant for HEMOSTAT?

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

What is the FDA product code for HEMOSTAT?

The FDA product code for HEMOSTAT is EMD.

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Other records listing Deringer-Ney, Inc. as applicant

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K933178GDC 3509K930482DENTAL CASTING ALLOY, MODIFICATION - PF-3K930481DENTAL CASTING ALLOY MODIFICATION-PF-4K925273GDC 3445K920922GDC 3367K920060DENTAL SOLDER ALLOY

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Related Devices (Code: EMD)

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.

K920883HEMOSTAT, SURGICAL (VARIOUS TYPES)S.T.S Instruments

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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