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FDA 510(k)

PREPACELL-BONE MARROW SAMPLER

K-Number: K791660 · 1979-09-12

ApplicantApplied Medical Devices, Inc.
Decision Date1979-09-12
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PREPACELL-BONE MARROW SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Devices, Inc.. It received FDA 510(k) clearance on 1979-09-12 under 510(k) number K791660. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREPACELL-BONE MARROW SAMPLER?

PREPACELL-BONE MARROW SAMPLER is a medical device that received FDA 510(k) clearance on 1979-09-12. The listed applicant is Applied Medical Devices, Inc.. The 510(k) number is K791660.

When did PREPACELL-BONE MARROW SAMPLER receive FDA 510(k) clearance?

PREPACELL-BONE MARROW SAMPLER received FDA 510(k) clearance on 1979-09-12, under 510(k) number K791660.

Who is the listed applicant for PREPACELL-BONE MARROW SAMPLER?

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

What is the FDA product code for PREPACELL-BONE MARROW SAMPLER?

The FDA product code for PREPACELL-BONE MARROW SAMPLER is FMF.

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Other records listing Applied Medical Devices, Inc. as applicant

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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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