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FDA 510(k)

SPECTRO C

K-Number: K872941 · 1987-09-04

ApplicantRamco Laboratories, Inc.
Decision Date1987-09-04
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SPECTRO C is the device name listed in this FDA 510(k) record. The listed applicant is Ramco Laboratories, Inc.. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K872941. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTRO C?

SPECTRO C is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is Ramco Laboratories, Inc.. The 510(k) number is K872941.

When did SPECTRO C receive FDA 510(k) clearance?

SPECTRO C received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872941.

Who is the listed applicant for SPECTRO C?

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

What is the FDA product code for SPECTRO C?

The FDA product code for SPECTRO C is GGP.

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Other records listing Ramco Laboratories, 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.

K983107VFEK981208TFRK910481EPO-RIAK864701VWF IMMUNOBLOTK861159SPECTRO VWFK831470PTH MR

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Related Devices (Code: GGP)

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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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