Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DRY-FORM

K-Number: K872663 · 1987-08-06

ApplicantAnatech, Ltd.
Decision Date1987-08-06
Product CodeIFP
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

DRY-FORM is the device name listed in this FDA 510(k) record. The listed applicant is Anatech, Ltd.. It received FDA 510(k) clearance on 1987-08-06 under 510(k) number K872663. The device is classified under product code IFP. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRY-FORM?

DRY-FORM is a medical device that received FDA 510(k) clearance on 1987-08-06. The listed applicant is Anatech, Ltd.. The 510(k) number is K872663.

When did DRY-FORM receive FDA 510(k) clearance?

DRY-FORM received FDA 510(k) clearance on 1987-08-06, under 510(k) number K872663.

Who is the listed applicant for DRY-FORM?

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

What is the FDA product code for DRY-FORM?

The FDA product code for DRY-FORM is IFP.

Other records listing Anatech, Ltd. 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.

K882874ZINC FORMALINK882873FIELDTEX HEMATOXYLINK882268ZINC FORMALIN CONCENTRATEK881282XYLENEK872498HARRIS HEMATOXYLINK872499ANATECH HEMATOXYLIN-NORMAL STRENGTH

View all 14 devices →

Related Devices (Code: IFP)

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.

K884755CONSED FECAL CONCENTRATION SYSTEMDonald L. Price, Ph.D.K872140(MSI) PATH-SAVERMedical Specialties, Inc.K870852NBF 10% NEUTRAL BUFFERED FORMALINAnatech, Ltd.K853497PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALINSurgipath Medical Industries, Inc.K842982FORMALIN BUFFEREDReagent Laboratory, Inc.K842940CBA FORMALINAnatech, Ltd.

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.

↑